Canonical Allele Identifier: CA3711793

Gene: HLA-B

Linked Data

• dbSNP Id: rs774183800
• ExAC: 6:31324541 CTGT / C
• gnomAD v2: 6-31324541-CTGT-C
• gnomAD v3: 6-31356764-CTGT-C
• gnomAD v4: 6-31356764-CTGT-C
• MyVariant Identifiers: chr6:g.31324542_31324544del (hg19) ; chr6:g.31356765_31356767del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356765_31356767del , CM000668.2:g.31356765_31356767del	GRCh38
NC_000006.11:g.31324542_31324544del , CM000668.1:g.31324542_31324544del	GRCh37
NC_000006.10:g.31432521_31432523del	NCBI36
NG_023187.1:g.5446_5448del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1737_1739del
ENST00000481849.6:n.1737_1739del
ENST00000497377.6:n.1737_1739del
ENST00000640094.2:c.264_266del	ENSP00000491275.2:p.Gln89del
ENST00000696558.1:c.264_266del	ENSP00000512716.1:p.Gln89del
ENST00000696559.1:c.264_266del	ENSP00000512717.1:p.Gln89del
ENST00000696560.1:c.264_266del	ENSP00000512718.1:p.Gln89del
ENST00000696561.1:c.264_266del	ENSP00000512719.1:p.Gln89del
ENST00000696562.1:c.264_266del	ENSP00000512720.1:p.Gln89del
ENST00000412585.7:c.264_266del MANE Select	ENSP00000399168.2:p.Gln89del
ENST00000412585.6:c.264_266del	ENSP00000399168.2:p.Gln89del
ENST00000434333.1:c.297_299del	ENSP00000405931.1:p.Gln100del
ENST00000474381.1:n.139_141del
ENST00000498007.1:n.285_287del
ENST00000603274.1:n.119_121del
NM_005514.6:c.264_266del	NP_005505.2:p.Gln89del
XM_011514556.1:c.297_299del	XP_011512858.1:p.Gln100del
XM_011514557.1:c.264_266del	XP_011512859.1:p.Gln89del
XR_926175.1:n.274_276del
NM_005514.7:c.264_266del	NP_005505.2:p.Gln89del
NM_005514.8:c.264_266del MANE Select	NP_005505.2:p.Gln89del