Canonical Allele Identifier: CA3711484

Gene: HLA-B

Linked Data

• dbSNP Id: rs773885164
• ExAC: 6:31323948 GC / G
• gnomAD v2: 6-31323948-GC-G
• MyVariant Identifiers: chr6:g.31323949del (hg19) ; chr6:g.31356172del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356172del , CM000668.2:g.31356172del	GRCh38
NC_000006.11:g.31323949del , CM000668.1:g.31323949del	GRCh37
NC_000006.10:g.31431928del	NCBI36
NG_023187.1:g.6041del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2087del
ENST00000481849.6:n.2087del
ENST00000497377.6:n.2087del
ENST00000640094.2:c.614del	ENSP00000491275.2:p.Arg205ProfsTer9
ENST00000696558.1:c.614del	ENSP00000512716.1:p.Arg205ProfsTer?
ENST00000696559.1:c.614del	ENSP00000512717.1:p.Arg205ProfsTer9
ENST00000696560.1:c.614del	ENSP00000512718.1:p.Arg205ProfsTer9
ENST00000696561.1:c.614del	ENSP00000512719.1:p.Arg205ProfsTer9
ENST00000696562.1:c.614del	ENSP00000512720.1:p.Arg205ProfsTer9
ENST00000412585.7:c.614del MANE Select	ENSP00000399168.2:p.Arg205ProfsTer9
ENST00000412585.6:c.614del	ENSP00000399168.2:p.Arg205ProfsTer9
ENST00000434333.1:c.647del	ENSP00000405931.1:p.Arg216ProfsTer9
ENST00000474381.1:n.489del
ENST00000498007.1:n.880del
NM_005514.6:c.614del	NP_005505.2:p.Arg205ProfsTer9
XM_011514556.1:c.647del	XP_011512858.1:p.Arg216ProfsTer9
XM_011514557.1:c.614del	XP_011512859.1:p.Arg205ProfsTer9
XR_926175.1:n.624del
NM_005514.7:c.614del	NP_005505.2:p.Arg205ProfsTer9
NM_005514.8:c.614del MANE Select	NP_005505.2:p.Arg205ProfsTer9