Canonical Allele Identifier: CA1619118295

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355163G= , CM000668.2:g.31355163G=	GRCh38
NC_000006.11:g.31322940G= , CM000668.1:g.31322940G=	GRCh37
NC_000006.10:g.31430919G=	NCBI36
NG_023187.1:g.7050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3003C=
ENST00000481849.6:n.2522C=
ENST00000497377.6:n.2429C=
ENST00000640094.2:c.895+154C=	ENSP00000491275.2:n.895+154C=
ENST00000696558.1:c.1025C=	ENSP00000512716.1:n.1025C=
ENST00000696559.1:c.956C=	ENSP00000512717.1:p.Ala319=
ENST00000696560.1:c.956C=	ENSP00000512718.1:p.Ala319=
ENST00000696561.1:c.956C=	ENSP00000512719.1:p.Ala319=
ENST00000696562.1:c.956C=	ENSP00000512720.1:p.Ala319=
ENST00000412585.7:c.956C= MANE Select	ENSP00000399168.2:p.Ala319=
ENST00000640094.1:c.88+154C=	ENSP00000491275.1:n.88+154C=
ENST00000412585.6:c.956C=	ENSP00000399168.2:p.Ala319=
ENST00000463574.1:n.547C=
NM_005514.6:c.956C=	NP_005505.2:p.Ala319=
XM_011514556.1:c.989C=	XP_011512858.1:p.Ala330=
XM_011514557.1:c.895+154C=	XP_011512859.1:n.895+154C=
XR_926175.1:n.1395C=
NM_005514.7:c.956C=	NP_005505.2:p.Ala319=
NM_005514.8:c.956C= MANE Select	NP_005505.2:p.Ala319=