Canonical Allele Identifier: CA1619118248

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355154A= , CM000668.2:g.31355154A=	GRCh38
NC_000006.11:g.31322931A= , CM000668.1:g.31322931A=	GRCh37
NC_000006.10:g.31430910A=	NCBI36
NG_023187.1:g.7059T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3012T=
ENST00000481849.6:n.2531T=
ENST00000497377.6:n.2438T=
ENST00000640094.2:c.895+163T=	ENSP00000491275.2:n.895+163T=
ENST00000696558.1:c.1034T=	ENSP00000512716.1:n.1034T=
ENST00000696559.1:c.965T=	ENSP00000512717.1:p.Val322=
ENST00000696560.1:c.965T=	ENSP00000512718.1:p.Val322=
ENST00000696561.1:c.965T=	ENSP00000512719.1:p.Val322=
ENST00000696562.1:c.965T=	ENSP00000512720.1:p.Val322=
ENST00000412585.7:c.965T= MANE Select	ENSP00000399168.2:p.Val322=
ENST00000640094.1:c.88+163T=	ENSP00000491275.1:n.88+163T=
ENST00000412585.6:c.965T=	ENSP00000399168.2:p.Val322=
ENST00000463574.1:n.556T=
NM_005514.6:c.965T=	NP_005505.2:p.Val322=
XM_011514556.1:c.998T=	XP_011512858.1:p.Val333=
XM_011514557.1:c.895+163T=	XP_011512859.1:n.895+163T=
XR_926175.1:n.1404T=
NM_005514.7:c.965T=	NP_005505.2:p.Val322=
NM_005514.8:c.965T= MANE Select	NP_005505.2:p.Val322=