Canonical Allele Identifier: CA1619113194

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356792C= , CM000668.2:g.31356792C=	GRCh38
NC_000006.11:g.31324569C= , CM000668.1:g.31324569C=	GRCh37
NC_000006.10:g.31432548C=	NCBI36
NG_023187.1:g.5421G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1712G=
ENST00000481849.6:n.1712G=
ENST00000497377.6:n.1712G=
ENST00000640094.2:c.239G=	ENSP00000491275.2:p.Gly80=
ENST00000696558.1:c.239G=	ENSP00000512716.1:p.Gly80=
ENST00000696559.1:c.239G=	ENSP00000512717.1:p.Gly80=
ENST00000696560.1:c.239G=	ENSP00000512718.1:p.Gly80=
ENST00000696561.1:c.239G=	ENSP00000512719.1:p.Gly80=
ENST00000696562.1:c.239G=	ENSP00000512720.1:p.Gly80=
ENST00000412585.7:c.239G= MANE Select	ENSP00000399168.2:p.Gly80=
ENST00000412585.6:c.239G=	ENSP00000399168.2:p.Gly80=
ENST00000434333.1:c.272G=	ENSP00000405931.1:p.Gly91=
ENST00000474381.1:n.114G=
ENST00000498007.1:n.260G=
ENST00000603274.1:n.146C=
NM_005514.6:c.239G=	NP_005505.2:p.Gly80=
XM_011514556.1:c.272G=	XP_011512858.1:p.Gly91=
XM_011514557.1:c.239G=	XP_011512859.1:p.Gly80=
XR_926175.1:n.249G=
NM_005514.7:c.239G=	NP_005505.2:p.Gly80=
NM_005514.8:c.239G= MANE Select	NP_005505.2:p.Gly80=