Canonical Allele Identifier: CA1619117215

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354498C= , CM000668.2:g.31354498C=	GRCh38
NC_000006.11:g.31322275C= , CM000668.1:g.31322275C=	GRCh37
NC_000006.10:g.31430254C=	NCBI36
NG_023187.1:g.7715G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3121G=
ENST00000481849.6:n.3081G=
ENST00000497377.6:n.2988G=
ENST00000640094.2:c.957G=	ENSP00000491275.2:p.Val319=
ENST00000696558.1:c.1143G=	ENSP00000512716.1:n.1143G=
ENST00000696559.1:c.1074G=	ENSP00000512717.1:p.Val358=
ENST00000696560.1:c.1074G=	ENSP00000512718.1:p.Val358=
ENST00000696561.1:c.1074G=	ENSP00000512719.1:p.Val358=
ENST00000696562.1:c.1074G=	ENSP00000512720.1:p.Val358=
ENST00000412585.7:c.1074G= MANE Select	ENSP00000399168.2:p.Val358=
ENST00000412585.6:c.1074G=	ENSP00000399168.2:p.Val358=
ENST00000481849.5:n.309G=
ENST00000497377.5:n.473G=
NM_005514.6:c.1074G=	NP_005505.2:p.Val358=
XM_011514556.1:c.1107G=	XP_011512858.1:p.Val369=
XM_011514557.1:c.957G=	XP_011512859.1:p.Val319=
XR_926175.1:n.1513G=
NM_005514.7:c.1074G=	NP_005505.2:p.Val358=
NM_005514.8:c.1074G= MANE Select	NP_005505.2:p.Val358=