Canonical Allele Identifier: CA1619116506
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354138A= , CM000668.2:g.31354138A= GRCh38
NC_000006.11:g.31321915A= , CM000668.1:g.31321915A= GRCh37
NC_000006.10:g.31429894A= NCBI36
NG_023187.1:g.8075T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3299T=
ENST00000481849.6:n.3259T=
ENST00000497377.6:n.3166T=
ENST00000696558.1:c.1321T= ENSP00000512716.1:n.1321T=
ENST00000696559.1:c.*163T= ENSP00000512717.1:n.*163T=
ENST00000696560.1:c.*163T= ENSP00000512718.1:n.*163T=
ENST00000696561.1:c.*163T= ENSP00000512719.1:n.*163T=
ENST00000696562.1:c.*163T= ENSP00000512720.1:n.*163T=
ENST00000412585.7:c.*163T= MANE Select ENSP00000399168.2:n.*163T=
ENST00000412585.6:c.*163T= ENSP00000399168.2:n.*163T=
ENST00000481849.5:n.487T=
ENST00000497377.5:n.651T=
NM_005514.6:c.*163T= NP_005505.2:n.*163T=
XM_011514556.1:c.*163T= XP_011512858.1:n.*163T=
XM_011514557.1:c.*163T= XP_011512859.1:n.*163T=
XR_926175.1:n.1691T=
NM_005514.7:c.*163T= NP_005505.2:n.*163T=
NM_005514.8:c.*163T= MANE Select NP_005505.2:n.*163T=