Canonical Allele Identifier: CA1619113204

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356795T= , CM000668.2:g.31356795T=	GRCh38
NC_000006.11:g.31324572T= , CM000668.1:g.31324572T=	GRCh37
NC_000006.10:g.31432551T=	NCBI36
NG_023187.1:g.5418A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1709A=
ENST00000481849.6:n.1709A=
ENST00000497377.6:n.1709A=
ENST00000640094.2:c.236A=	ENSP00000491275.2:p.Glu79=
ENST00000696558.1:c.236A=	ENSP00000512716.1:p.Glu79=
ENST00000696559.1:c.236A=	ENSP00000512717.1:p.Glu79=
ENST00000696560.1:c.236A=	ENSP00000512718.1:p.Glu79=
ENST00000696561.1:c.236A=	ENSP00000512719.1:p.Glu79=
ENST00000696562.1:c.236A=	ENSP00000512720.1:p.Glu79=
ENST00000412585.7:c.236A= MANE Select	ENSP00000399168.2:p.Glu79=
ENST00000412585.6:c.236A=	ENSP00000399168.2:p.Glu79=
ENST00000434333.1:c.269A=	ENSP00000405931.1:p.Glu90=
ENST00000474381.1:n.111A=
ENST00000498007.1:n.257A=
ENST00000603274.1:n.149T=
NM_005514.6:c.236A=	NP_005505.2:p.Glu79=
XM_011514556.1:c.269A=	XP_011512858.1:p.Glu90=
XM_011514557.1:c.236A=	XP_011512859.1:p.Glu79=
XR_926175.1:n.246A=
NM_005514.7:c.236A=	NP_005505.2:p.Glu79=
NM_005514.8:c.236A= MANE Select	NP_005505.2:p.Glu79=