Canonical Allele Identifier: CA1619117319

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354538C= , CM000668.2:g.31354538C=	GRCh38
NC_000006.11:g.31322315C= , CM000668.1:g.31322315C=	GRCh37
NC_000006.10:g.31430294C=	NCBI36
NG_023187.1:g.7675G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3093-12G=
ENST00000481849.6:n.3053-12G=
ENST00000497377.6:n.2960-12G=
ENST00000640094.2:c.929-12G=	ENSP00000491275.2:n.929-12G=
ENST00000696558.1:c.1115-12G=	ENSP00000512716.1:n.1115-12G=
ENST00000696559.1:c.1046-12G=	ENSP00000512717.1:n.1046-12G=
ENST00000696560.1:c.1046-12G=	ENSP00000512718.1:n.1046-12G=
ENST00000696561.1:c.1046-12G=	ENSP00000512719.1:n.1046-12G=
ENST00000696562.1:c.1046-12G=	ENSP00000512720.1:n.1046-12G=
ENST00000412585.7:c.1046-12G= MANE Select	ENSP00000399168.2:n.1046-12G=
ENST00000640094.1:c.122-12G=	ENSP00000491275.1:n.122-12G=
ENST00000412585.6:c.1046-12G=	ENSP00000399168.2:n.1046-12G=
ENST00000481849.5:n.269G=
ENST00000497377.5:n.445-12G=
NM_005514.6:c.1046-12G=	NP_005505.2:n.1046-12G=
XM_011514556.1:c.1079-12G=	XP_011512858.1:n.1079-12G=
XM_011514557.1:c.929-12G=	XP_011512859.1:n.929-12G=
XR_926175.1:n.1485-12G=
NM_005514.7:c.1046-12G=	NP_005505.2:n.1046-12G=
NM_005514.8:c.1046-12G= MANE Select	NP_005505.2:n.1046-12G=