Canonical Allele Identifier: CA2770503694
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356192_31356193insGACGGCAGCGACAGTGCGCGCGAGAAGCTCACGAGC , CM000668.2:g.31356192_31356193insGACGGCAGCGACAGTGCGCGCGAGAAGCTCACGAGC GRCh38
NC_000006.11:g.31323969_31323970insGACGGCAGCGACAGTGCGCGCGAGAAGCTCACGAGC , CM000668.1:g.31323969_31323970insGACGGCAGCGACAGTGCGCGCGAGAAGCTCACGAGC GRCh37
NC_000006.10:g.31431948_31431949insGACGGCAGCGACAGTGCGCGCGAGAAGCTCACGAGC NCBI36
NG_023187.1:g.6020_6021insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2066_2067insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC
ENST00000481849.6:n.2066_2067insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC
ENST00000497377.6:n.2066_2067insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC
ENST00000640094.2:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000491275.2:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000696558.1:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000512716.1:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000696559.1:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000512717.1:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000696560.1:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000512718.1:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000696561.1:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000512719.1:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000696562.1:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000512720.1:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000412585.7:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC MANE Select ENSP00000399168.2:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000412585.6:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000399168.2:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000434333.1:c.626_627insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC ENSP00000405931.1:p.Asn209delinsLysLeuValSerPheSerArgAlaLeuSe...
ENST00000474381.1:n.468_469insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC
ENST00000498007.1:n.859_860insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC
NM_005514.6:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC NP_005505.2:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSerLeuPr...
XM_011514556.1:c.626_627insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC XP_011512858.1:p.Asn209delinsLysLeuValSerPheSerArgAlaLeuSerLe...
XM_011514557.1:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC XP_011512859.1:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSerLe...
XR_926175.1:n.603_604insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC
NM_005514.7:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC NP_005505.2:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSerLeuPr...
NM_005514.8:c.593_594insGCTCGTGAGCTTCTCGCGCGCACTGTCGCTGCCGTC MANE Select NP_005505.2:p.Asn198delinsLysLeuValSerPheSerArgAlaLeuSerLeuPr...