Canonical Allele Identifier: CA2677956590

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356241-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356245_31356246del , CM000668.2:g.31356245_31356246del	GRCh38
NC_000006.11:g.31324022_31324023del , CM000668.1:g.31324022_31324023del	GRCh37
NC_000006.10:g.31432001_31432002del	NCBI36
NG_023187.1:g.5970_5971del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2016_2017del
ENST00000481849.6:n.2016_2017del
ENST00000497377.6:n.2016_2017del
ENST00000640094.2:c.543_544del	ENSP00000491275.2:p.Arg181SerfsTer26
ENST00000696558.1:c.543_544del	ENSP00000512716.1:p.Arg181SerfsTer26
ENST00000696559.1:c.543_544del	ENSP00000512717.1:p.Arg181SerfsTer26
ENST00000696560.1:c.543_544del	ENSP00000512718.1:p.Arg181SerfsTer26
ENST00000696561.1:c.543_544del	ENSP00000512719.1:p.Arg181SerfsTer26
ENST00000696562.1:c.543_544del	ENSP00000512720.1:p.Arg181SerfsTer26
ENST00000412585.7:c.543_544del MANE Select	ENSP00000399168.2:p.Arg181SerfsTer26
ENST00000412585.6:c.543_544del	ENSP00000399168.2:p.Arg181SerfsTer26
ENST00000434333.1:c.576_577del	ENSP00000405931.1:p.Arg192SerfsTer26
ENST00000474381.1:n.418_419del
ENST00000498007.1:n.809_810del
NM_005514.6:c.543_544del	NP_005505.2:p.Arg181SerfsTer26
XM_011514556.1:c.576_577del	XP_011512858.1:p.Arg192SerfsTer26
XM_011514557.1:c.543_544del	XP_011512859.1:p.Arg181SerfsTer26
XR_926175.1:n.553_554del
NM_005514.7:c.543_544del	NP_005505.2:p.Arg181SerfsTer26
NM_005514.8:c.543_544del MANE Select	NP_005505.2:p.Arg181SerfsTer26