Canonical Allele Identifier: CA1619117267

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354512G= , CM000668.2:g.31354512G=	GRCh38
NC_000006.11:g.31322289G= , CM000668.1:g.31322289G=	GRCh37
NC_000006.10:g.31430268G=	NCBI36
NG_023187.1:g.7701C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3107C=
ENST00000481849.6:n.3067C=
ENST00000497377.6:n.2974C=
ENST00000640094.2:c.943C=	ENSP00000491275.2:p.Gln315=
ENST00000696558.1:c.1129C=	ENSP00000512716.1:n.1129C=
ENST00000696559.1:c.1060C=	ENSP00000512717.1:p.Gln354=
ENST00000696560.1:c.1060C=	ENSP00000512718.1:p.Gln354=
ENST00000696561.1:c.1060C=	ENSP00000512719.1:p.Gln354=
ENST00000696562.1:c.1060C=	ENSP00000512720.1:p.Gln354=
ENST00000412585.7:c.1060C= MANE Select	ENSP00000399168.2:p.Gln354=
ENST00000640094.1:c.136C=	ENSP00000491275.1:p.Gln46=
ENST00000412585.6:c.1060C=	ENSP00000399168.2:p.Gln354=
ENST00000481849.5:n.295C=
ENST00000497377.5:n.459C=
NM_005514.6:c.1060C=	NP_005505.2:p.Gln354=
XM_011514556.1:c.1093C=	XP_011512858.1:p.Gln365=
XM_011514557.1:c.943C=	XP_011512859.1:p.Gln315=
XR_926175.1:n.1499C=
NM_005514.7:c.1060C=	NP_005505.2:p.Gln354=
NM_005514.8:c.1060C= MANE Select	NP_005505.2:p.Gln354=