Canonical Allele Identifier: CA1619118337

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355191C= , CM000668.2:g.31355191C=	GRCh38
NC_000006.11:g.31322968C= , CM000668.1:g.31322968C=	GRCh37
NC_000006.10:g.31430947C=	NCBI36
NG_023187.1:g.7022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2975G=
ENST00000481849.6:n.2494G=
ENST00000497377.6:n.2401G=
ENST00000640094.2:c.895+126G=	ENSP00000491275.2:n.895+126G=
ENST00000696558.1:c.997G=	ENSP00000512716.1:n.997G=
ENST00000696559.1:c.928G=	ENSP00000512717.1:p.Gly310=
ENST00000696560.1:c.928G=	ENSP00000512718.1:p.Gly310=
ENST00000696561.1:c.928G=	ENSP00000512719.1:p.Gly310=
ENST00000696562.1:c.928G=	ENSP00000512720.1:p.Gly310=
ENST00000412585.7:c.928G= MANE Select	ENSP00000399168.2:p.Gly310=
ENST00000640094.1:c.88+126G=	ENSP00000491275.1:n.88+126G=
ENST00000412585.6:c.928G=	ENSP00000399168.2:p.Gly310=
ENST00000463574.1:n.519G=
NM_005514.6:c.928G=	NP_005505.2:p.Gly310=
XM_011514556.1:c.961G=	XP_011512858.1:p.Gly321=
XM_011514557.1:c.895+126G=	XP_011512859.1:n.895+126G=
XR_926175.1:n.1367G=
NM_005514.7:c.928G=	NP_005505.2:p.Gly310=
NM_005514.8:c.928G= MANE Select	NP_005505.2:p.Gly310=