Canonical Allele Identifier: CA1619114436

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357175A= , CM000668.2:g.31357175A=	GRCh38
NC_000006.11:g.31324952A= , CM000668.1:g.31324952A=	GRCh37
NC_000006.10:g.31432931A=	NCBI36
NG_023187.1:g.5038T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1457T=
ENST00000481849.6:n.1457T=
ENST00000497377.6:n.1457T=
ENST00000696559.1:c.-17T=	ENSP00000512717.1:n.-17T=
ENST00000696560.1:c.-17T=	ENSP00000512718.1:n.-17T=
ENST00000696561.1:c.-17T=	ENSP00000512719.1:n.-17T=
ENST00000696562.1:c.-17T=	ENSP00000512720.1:n.-17T=
ENST00000412585.7:c.-17T= MANE Select	ENSP00000399168.2:n.-17T=
ENST00000412585.6:c.-17T=	ENSP00000399168.2:n.-17T=
ENST00000434333.1:c.-112T=	ENSP00000405931.1:n.-112T=
ENST00000498007.1:n.5T=
ENST00000603274.1:n.529A=
NM_005514.6:c.-17T=	NP_005505.2:n.-17T=
NM_005514.7:c.-17T=	NP_005505.2:n.-17T=
NM_005514.8:c.-17T= MANE Select	NP_005505.2:n.-17T=