Canonical Allele Identifier: CA2770503695
Gene: HLA-B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356192_31356193insGACGGTAGCGACAGTGCGCGCGAGAAGCTCACGAGCTTGCGTGACAGTTTGACCTCTGCGGCAACGGATATGCGAGA , CM000668.2:g.31356192_31356193insGACGGTAGCGACAGTGCGCGCGAGAAGCTCACGAGCTTGCGTGACAGTTTGACCTCTGCGGCAACGGATATGCGAGA GRCh38
NC_000006.11:g.31323969_31323970insGACGGTAGCGACAGTGCGCGCGAGAAGCTCACGAGCTTGCGTGACAGTTTGACCTCTGCGGCAACGGATATGCGAGA , CM000668.1:g.31323969_31323970insGACGGTAGCGACAGTGCGCGCGAGAAGCTCACGAGCTTGCGTGACAGTTTGACCTCTGCGGCAACGGATATGCGAGA GRCh37
NC_000006.10:g.31431948_31431949insGACGGTAGCGACAGTGCGCGCGAGAAGCTCACGAGCTTGCGTGACAGTTTGACCTCTGCGGCAACGGATATGCGAGA NCBI36
NG_023187.1:g.6020_6021insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2066_2067insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC
ENST00000481849.6:n.2066_2067insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC
ENST00000497377.6:n.2066_2067insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC
ENST00000640094.2:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000491275.2:p.Gly199LeufsTer16
ENST00000696558.1:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000512716.1:p.Gly199LeufsTer16
ENST00000696559.1:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000512717.1:p.Gly199LeufsTer16
ENST00000696560.1:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000512718.1:p.Gly199LeufsTer16
ENST00000696561.1:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000512719.1:p.Gly199LeufsTer16
ENST00000696562.1:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000512720.1:p.Gly199LeufsTer16
ENST00000412585.7:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC MANE Select ENSP00000399168.2:p.Gly199LeufsTer16
ENST00000412585.6:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000399168.2:p.Gly199LeufsTer16
ENST00000434333.1:c.626_627insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC ENSP00000405931.1:p.Gly210LeufsTer16
ENST00000474381.1:n.468_469insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC
ENST00000498007.1:n.859_860insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC
NM_005514.6:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC NP_005505.2:p.Gly199LeufsTer16
XM_011514556.1:c.626_627insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC XP_011512858.1:p.Gly210LeufsTer16
XM_011514557.1:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC XP_011512859.1:p.Gly199LeufsTer16
XR_926175.1:n.603_604insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC
NM_005514.7:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC NP_005505.2:p.Gly199LeufsTer16
NM_005514.8:c.593_594insTCTCGCATATCCGTTGCCGCAGAGGTCAAACTGTCACGCAAGCTCGTGAGCTTCTCGCGCGCACTGTCGCTACCGTC MANE Select NP_005505.2:p.Gly199LeufsTer16
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