Canonical Allele Identifier: CA2677956592

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356243-TCTCCGCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356250_31356257del , CM000668.2:g.31356250_31356257del	GRCh38
NC_000006.11:g.31324027_31324034del , CM000668.1:g.31324027_31324034del	GRCh37
NC_000006.10:g.31432006_31432013del	NCBI36
NG_023187.1:g.5962_5969del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2008_2015del
ENST00000481849.6:n.2008_2015del
ENST00000497377.6:n.2008_2015del
ENST00000640094.2:c.535_542del	ENSP00000491275.2:p.Gln179SerfsTer26
ENST00000696558.1:c.535_542del	ENSP00000512716.1:p.Gln179SerfsTer26
ENST00000696559.1:c.535_542del	ENSP00000512717.1:p.Gln179SerfsTer26
ENST00000696560.1:c.535_542del	ENSP00000512718.1:p.Gln179SerfsTer26
ENST00000696561.1:c.535_542del	ENSP00000512719.1:p.Gln179SerfsTer26
ENST00000696562.1:c.535_542del	ENSP00000512720.1:p.Gln179SerfsTer26
ENST00000412585.7:c.535_542del MANE Select	ENSP00000399168.2:p.Gln179SerfsTer26
ENST00000412585.6:c.535_542del	ENSP00000399168.2:p.Gln179SerfsTer26
ENST00000434333.1:c.568_575del	ENSP00000405931.1:p.Gln190SerfsTer26
ENST00000474381.1:n.410_417del
ENST00000498007.1:n.801_808del
NM_005514.6:c.535_542del	NP_005505.2:p.Gln179SerfsTer26
XM_011514556.1:c.568_575del	XP_011512858.1:p.Gln190SerfsTer26
XM_011514557.1:c.535_542del	XP_011512859.1:p.Gln179SerfsTer26
XR_926175.1:n.545_552del
NM_005514.7:c.535_542del	NP_005505.2:p.Gln179SerfsTer26
NM_005514.8:c.535_542del MANE Select	NP_005505.2:p.Gln179SerfsTer26