Canonical Allele Identifier: CA1619119455

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355760G= , CM000668.2:g.31355760G=	GRCh38
NC_000006.11:g.31323537G= , CM000668.1:g.31323537G=	GRCh37
NC_000006.10:g.31431516G=	NCBI36
NG_023187.1:g.6453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2499C=
ENST00000481849.6:n.2093-168C=
ENST00000497377.6:n.2093-168C=
ENST00000640094.2:c.620-168C=	ENSP00000491275.2:n.620-168C=
ENST00000696558.1:c.666C=	ENSP00000512716.1:p.Ser222=
ENST00000696559.1:c.620-168C=	ENSP00000512717.1:n.620-168C=
ENST00000696560.1:c.620-168C=	ENSP00000512718.1:n.620-168C=
ENST00000696561.1:c.620-168C=	ENSP00000512719.1:n.620-168C=
ENST00000696562.1:c.620-168C=	ENSP00000512720.1:n.620-168C=
ENST00000412585.7:c.620-168C= MANE Select	ENSP00000399168.2:n.620-168C=
ENST00000412585.6:c.620-168C=	ENSP00000399168.2:n.620-168C=
ENST00000434333.1:c.653-168C=	ENSP00000405931.1:n.653-168C=
ENST00000463574.1:n.43C=
ENST00000474381.1:n.901C=
ENST00000498007.1:n.886-168C=
NM_005514.6:c.620-168C=	NP_005505.2:n.620-168C=
XM_011514556.1:c.653-168C=	XP_011512858.1:n.653-168C=
XM_011514557.1:c.620-168C=	XP_011512859.1:n.620-168C=
XR_926175.1:n.1036C=
NM_005514.7:c.620-168C=	NP_005505.2:n.620-168C=
NM_005514.8:c.620-168C= MANE Select	NP_005505.2:n.620-168C=