Canonical Allele Identifier: CA1619118266

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355157A= , CM000668.2:g.31355157A=	GRCh38
NC_000006.11:g.31322934A= , CM000668.1:g.31322934A=	GRCh37
NC_000006.10:g.31430913A=	NCBI36
NG_023187.1:g.7056T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3009T=
ENST00000481849.6:n.2528T=
ENST00000497377.6:n.2435T=
ENST00000640094.2:c.895+160T=	ENSP00000491275.2:n.895+160T=
ENST00000696558.1:c.1031T=	ENSP00000512716.1:n.1031T=
ENST00000696559.1:c.962T=	ENSP00000512717.1:p.Val321=
ENST00000696560.1:c.962T=	ENSP00000512718.1:p.Val321=
ENST00000696561.1:c.962T=	ENSP00000512719.1:p.Val321=
ENST00000696562.1:c.962T=	ENSP00000512720.1:p.Val321=
ENST00000412585.7:c.962T= MANE Select	ENSP00000399168.2:p.Val321=
ENST00000640094.1:c.88+160T=	ENSP00000491275.1:n.88+160T=
ENST00000412585.6:c.962T=	ENSP00000399168.2:p.Val321=
ENST00000463574.1:n.553T=
NM_005514.6:c.962T=	NP_005505.2:p.Val321=
XM_011514556.1:c.995T=	XP_011512858.1:p.Val332=
XM_011514557.1:c.895+160T=	XP_011512859.1:n.895+160T=
XR_926175.1:n.1401T=
NM_005514.7:c.962T=	NP_005505.2:p.Val321=
NM_005514.8:c.962T= MANE Select	NP_005505.2:p.Val321=