Canonical Allele Identifier: CA2571169061

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354872C>G , CM000668.2:g.31354872C>G	GRCh38
NC_000006.11:g.31322649C>G , CM000668.1:g.31322649C>G	GRCh37
NC_000006.10:g.31430628C>G	NCBI36
NG_023187.1:g.7341G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3060-207G>C
ENST00000481849.6:n.2813G>C
ENST00000497377.6:n.2720G>C
ENST00000640094.2:c.896-207G>C	ENSP00000491275.2:n.896-207G>C
ENST00000696558.1:c.1082-207G>C	ENSP00000512716.1:n.1082-207G>C
ENST00000696559.1:c.1013-207G>C	ENSP00000512717.1:n.1013-207G>C
ENST00000696560.1:c.1013-207G>C	ENSP00000512718.1:n.1013-207G>C
ENST00000696561.1:c.1013-207G>C	ENSP00000512719.1:n.1013-207G>C
ENST00000696562.1:c.1013-207G>C	ENSP00000512720.1:n.1013-207G>C
ENST00000412585.7:c.1013-207G>C MANE Select	ENSP00000399168.2:n.1013-207G>C
ENST00000640094.1:c.89-207G>C	ENSP00000491275.1:n.89-207G>C
ENST00000412585.6:c.1013-207G>C	ENSP00000399168.2:n.1013-207G>C
ENST00000497377.5:n.205G>C
NM_005514.6:c.1013-207G>C	NP_005505.2:n.1013-207G>C
XM_011514556.1:c.1046-207G>C	XP_011512858.1:n.1046-207G>C
XM_011514557.1:c.896-207G>C	XP_011512859.1:n.896-207G>C
XR_926175.1:n.1452-207G>C
NM_005514.7:c.1013-207G>C	NP_005505.2:n.1013-207G>C
NM_005514.8:c.1013-207G>C MANE Select	NP_005505.2:n.1013-207G>C