When several alleles are shown, the nucleotide mutations and amino acid changes for a given codon are indicated in red letters. These polymorphic mutations are reported in Tables of alleles.
Dashes indicate identical nucleotides. Dots indicate gaps according to the IMGT unique numbering. Blanks indicate partial sequences (blanks at the 5' and/or 3' end).

                                                               
                                         1   2   3   4   5   6   7   8   9   10  11  12  13  14  15  16  17  18  19  20 
                                         Q   E   Q   L   E   E   S   G   G       H   L   V   T   P   G   G   S   L   T 
  M60121   IGHV1S37*01 P  (1)           cag gag cag ctg gag gag tcc ggg ggt ... cac ctg gtc acg cct gga gga tcc ctg aca


                                                                ___________________CDR1-IMGT____________________        
                                     
                                         21  22  23  24  25  26  27  28  29  30  31  32  33  34  35  36  37  38  39  40 
                                         L   T   C   T   A   S   G   F   S   L                   S   S   Y   N   M   G 
  M60121   IGHV1S37*01 P  (1)           ctc acc tgc aca gcc tct gga ttc tcc ctc ... ... ... ... agt agc tac aac atg ggc


                                                                                                    _______________CDR2-

                                     
                                         41  42  43  44  45  46  47  48  49  50  51  52  53  54  55  56  57  58  59  60 
                                         W   V   R   Q   A   P   G   K   G   L   E   Y   I   G   Y   I   S   S   A     
  M60121   IGHV1S37*01 P (1)            tgg gtc cgc cag gct cca ggg aag ggg ctg gaa tac atc gga tat ata agt agt gct ...


                                        IMGT________________                                                            
                                     
                                         61  62  63  64  65  66  67  68  69  70  71  72  73  74  75  76  77  78  79  80 
                                                 G   S   T   Y   Y   A   S   W   V   N       G   R   F   T   I   S   K 
  M60121   IGHV1S37*01 P (1)            ... ... ggt agc aca tac tac gcg agc tgg gtg aat ... ggt cga ttc acc atc tcc aaa


                                     
                                     
                                         81  82  83  84  85  86  87  88  89  90  91  92  93  94  95  96  97  98  99 100 
                                         T   S   T           T   M   D   L   K   M   N   S   P   T   A   S   D   T   A 
  M60121   IGHV1S37*01 P (1)            acc tcg acc ... ... acg atg gat ctg aaa atg aac agt ccg aca gcc tcg gac acg gcc


                                                        CDR3-IMGT    
                                     
                                        101 102 103 104 105 106 

                                         T   Y   F   C   A   R  
  M60121   IGHV1S37*01 P (1)            acc tat ttc tgt gcc aga ga

This alignment of allele is generated by IMGT/OutilAllele.

IMGT note:
(1) Pseudogene because deletion of 1 nucleotide found in L-PART1.