Canonical Allele Identifier: CA1619117565

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354665C= , CM000668.2:g.31354665C=	GRCh38
NC_000006.11:g.31322442C= , CM000668.1:g.31322442C=	GRCh37
NC_000006.10:g.31430421C=	NCBI36
NG_023187.1:g.7548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3060G=
ENST00000481849.6:n.3020G=
ENST00000497377.6:n.2927G=
ENST00000640094.2:c.896G=	ENSP00000491275.2:p.Gly299=
ENST00000696558.1:c.1082G=	ENSP00000512716.1:n.1082G=
ENST00000696559.1:c.1013G=	ENSP00000512717.1:p.Gly338=
ENST00000696560.1:c.1013G=	ENSP00000512718.1:p.Gly338=
ENST00000696561.1:c.1013G=	ENSP00000512719.1:p.Gly338=
ENST00000696562.1:c.1013G=	ENSP00000512720.1:p.Gly338=
ENST00000412585.7:c.1013G= MANE Select	ENSP00000399168.2:p.Gly338=
ENST00000640094.1:c.89G=	ENSP00000491275.1:p.Gly30=
ENST00000412585.6:c.1013G=	ENSP00000399168.2:p.Gly338=
ENST00000481849.5:n.142G=
ENST00000497377.5:n.412G=
NM_005514.6:c.1013G=	NP_005505.2:p.Gly338=
XM_011514556.1:c.1046G=	XP_011512858.1:p.Gly349=
XM_011514557.1:c.896G=	XP_011512859.1:p.Gly299=
XR_926175.1:n.1452G=
NM_005514.7:c.1013G=	NP_005505.2:p.Gly338=
NM_005514.8:c.1013G= MANE Select	NP_005505.2:p.Gly338=