Canonical Allele Identifier: CA1619117514

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354637A= , CM000668.2:g.31354637A=	GRCh38
NC_000006.11:g.31322414A= , CM000668.1:g.31322414A=	GRCh37
NC_000006.10:g.31430393A=	NCBI36
NG_023187.1:g.7576T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3088T=
ENST00000481849.6:n.3048T=
ENST00000497377.6:n.2955T=
ENST00000640094.2:c.924T=	ENSP00000491275.2:p.Ala308=
ENST00000696558.1:c.1110T=	ENSP00000512716.1:n.1110T=
ENST00000696559.1:c.1041T=	ENSP00000512717.1:p.Ala347=
ENST00000696560.1:c.1041T=	ENSP00000512718.1:p.Ala347=
ENST00000696561.1:c.1041T=	ENSP00000512719.1:p.Ala347=
ENST00000696562.1:c.1041T=	ENSP00000512720.1:p.Ala347=
ENST00000412585.7:c.1041T= MANE Select	ENSP00000399168.2:p.Ala347=
ENST00000640094.1:c.117T=	ENSP00000491275.1:p.Ala39=
ENST00000412585.6:c.1041T=	ENSP00000399168.2:p.Ala347=
ENST00000481849.5:n.170T=
ENST00000497377.5:n.440T=
NM_005514.6:c.1041T=	NP_005505.2:p.Ala347=
XM_011514556.1:c.1074T=	XP_011512858.1:p.Ala358=
XM_011514557.1:c.924T=	XP_011512859.1:p.Ala308=
XR_926175.1:n.1480T=
NM_005514.7:c.1041T=	NP_005505.2:p.Ala347=
NM_005514.8:c.1041T= MANE Select	NP_005505.2:p.Ala347=