Canonical Allele Identifier: CA1619117868
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354923A= , CM000668.2:g.31354923A= GRCh38
NC_000006.11:g.31322700A= , CM000668.1:g.31322700A= GRCh37
NC_000006.10:g.31430679A= NCBI36
NG_023187.1:g.7290T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3059+184T=
ENST00000481849.6:n.2762T=
ENST00000497377.6:n.2669T=
ENST00000640094.2:c.896-258T= ENSP00000491275.2:n.896-258T=
ENST00000696558.1:c.1081+184T= ENSP00000512716.1:n.1081+184T=
ENST00000696559.1:c.1012+184T= ENSP00000512717.1:n.1012+184T=
ENST00000696560.1:c.1012+184T= ENSP00000512718.1:n.1012+184T=
ENST00000696561.1:c.1012+184T= ENSP00000512719.1:n.1012+184T=
ENST00000696562.1:c.1012+184T= ENSP00000512720.1:n.1012+184T=
ENST00000412585.7:c.1012+184T= MANE Select ENSP00000399168.2:n.1012+184T=
ENST00000640094.1:c.89-258T= ENSP00000491275.1:n.89-258T=
ENST00000412585.6:c.1012+184T= ENSP00000399168.2:n.1012+184T=
ENST00000497377.5:n.154T=
NM_005514.6:c.1012+184T= NP_005505.2:n.1012+184T=
XM_011514556.1:c.1045+184T= XP_011512858.1:n.1045+184T=
XM_011514557.1:c.896-258T= XP_011512859.1:n.896-258T=
XR_926175.1:n.1451+184T=
NM_005514.7:c.1012+184T= NP_005505.2:n.1012+184T=
NM_005514.8:c.1012+184T= MANE Select NP_005505.2:n.1012+184T=