Canonical Allele Identifier: CA1619117551

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354656C= , CM000668.2:g.31354656C=	GRCh38
NC_000006.11:g.31322433C= , CM000668.1:g.31322433C=	GRCh37
NC_000006.10:g.31430412C=	NCBI36
NG_023187.1:g.7557G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3069G=
ENST00000481849.6:n.3029G=
ENST00000497377.6:n.2936G=
ENST00000640094.2:c.905G=	ENSP00000491275.2:p.Gly302=
ENST00000696558.1:c.1091G=	ENSP00000512716.1:n.1091G=
ENST00000696559.1:c.1022G=	ENSP00000512717.1:p.Gly341=
ENST00000696560.1:c.1022G=	ENSP00000512718.1:p.Gly341=
ENST00000696561.1:c.1022G=	ENSP00000512719.1:p.Gly341=
ENST00000696562.1:c.1022G=	ENSP00000512720.1:p.Gly341=
ENST00000412585.7:c.1022G= MANE Select	ENSP00000399168.2:p.Gly341=
ENST00000640094.1:c.98G=	ENSP00000491275.1:p.Gly33=
ENST00000412585.6:c.1022G=	ENSP00000399168.2:p.Gly341=
ENST00000481849.5:n.151G=
ENST00000497377.5:n.421G=
NM_005514.6:c.1022G=	NP_005505.2:p.Gly341=
XM_011514556.1:c.1055G=	XP_011512858.1:p.Gly352=
XM_011514557.1:c.905G=	XP_011512859.1:p.Gly302=
XR_926175.1:n.1461G=
NM_005514.7:c.1022G=	NP_005505.2:p.Gly341=
NM_005514.8:c.1022G= MANE Select	NP_005505.2:p.Gly341=