Canonical Allele Identifier: CA2677955105
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355209_31355210insATAGAT , CM000668.2:g.31355209_31355210insATAGAT GRCh38
NC_000006.11:g.31322986_31322987insATAGAT , CM000668.1:g.31322986_31322987insATAGAT GRCh37
NC_000006.10:g.31430965_31430966insATAGAT NCBI36
NG_023187.1:g.7003_7004insATCTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2956_2957insATCTAT
ENST00000481849.6:n.2475_2476insATCTAT
ENST00000497377.6:n.2382_2383insATCTAT
ENST00000640094.2:c.895+107_895+108insATCTAT ENSP00000491275.2:n.895+107_895+108insATCTAT
ENST00000696558.1:c.978_979insATCTAT ENSP00000512716.1:n.978_979insATCTAT
ENST00000696559.1:c.909_910insATCTAT ENSP00000512717.1:p.Gln303_Ser304insIleTyr
ENST00000696560.1:c.909_910insATCTAT ENSP00000512718.1:p.Gln303_Ser304insIleTyr
ENST00000696561.1:c.909_910insATCTAT ENSP00000512719.1:p.Gln303_Ser304insIleTyr
ENST00000696562.1:c.909_910insATCTAT ENSP00000512720.1:p.Gln303_Ser304insIleTyr
ENST00000412585.7:c.909_910insATCTAT MANE Select ENSP00000399168.2:p.Gln303_Ser304insIleTyr
ENST00000640094.1:c.88+107_88+108insATCTAT ENSP00000491275.1:n.88+107_88+108insATCTAT
ENST00000412585.6:c.909_910insATCTAT ENSP00000399168.2:p.Gln303_Ser304insIleTyr
ENST00000463574.1:n.500_501insATCTAT
NM_005514.6:c.909_910insATCTAT NP_005505.2:p.Gln303_Ser304insIleTyr
XM_011514556.1:c.942_943insATCTAT XP_011512858.1:p.Gln314_Ser315insIleTyr
XM_011514557.1:c.895+107_895+108insATCTAT XP_011512859.1:n.895+107_895+108insATCTAT
XR_926175.1:n.1348_1349insATCTAT
NM_005514.7:c.909_910insATCTAT NP_005505.2:p.Gln303_Ser304insIleTyr
NM_005514.8:c.909_910insATCTAT MANE Select NP_005505.2:p.Gln303_Ser304insIleTyr