Canonical Allele Identifier: CA2770503680

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356168_31356169insC , CM000668.2:g.31356168_31356169insC	GRCh38
NC_000006.11:g.31323945_31323946insC , CM000668.1:g.31323945_31323946insC	GRCh37
NC_000006.10:g.31431924_31431925insC	NCBI36
NG_023187.1:g.6044_6045insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2090_2091insG
ENST00000481849.6:n.2090_2091insG
ENST00000497377.6:n.2090_2091insG
ENST00000640094.2:c.617_618insG	ENSP00000491275.2:p.Asp207Ter
ENST00000696558.1:c.617_618insG	ENSP00000512716.1:p.Asp207Ter
ENST00000696559.1:c.617_618insG	ENSP00000512717.1:p.Asp207Ter
ENST00000696560.1:c.617_618insG	ENSP00000512718.1:p.Asp207Ter
ENST00000696561.1:c.617_618insG	ENSP00000512719.1:p.Asp207Ter
ENST00000696562.1:c.617_618insG	ENSP00000512720.1:p.Asp207Ter
ENST00000412585.7:c.617_618insG MANE Select	ENSP00000399168.2:p.Asp207Ter
ENST00000412585.6:c.617_618insG	ENSP00000399168.2:p.Asp207Ter
ENST00000434333.1:c.650_651insG	ENSP00000405931.1:p.Asp218Ter
ENST00000474381.1:n.492_493insG
ENST00000498007.1:n.883_884insG
NM_005514.6:c.617_618insG	NP_005505.2:p.Asp207Ter
XM_011514556.1:c.650_651insG	XP_011512858.1:p.Asp218Ter
XM_011514557.1:c.617_618insG	XP_011512859.1:p.Asp207Ter
XR_926175.1:n.627_628insG
NM_005514.7:c.617_618insG	NP_005505.2:p.Asp207Ter
NM_005514.8:c.617_618insG MANE Select	NP_005505.2:p.Asp207Ter