Canonical Allele Identifier: CA136835950

Gene: HLA-B

Linked Data

• dbSNP Id: rs151341232
• gnomAD v4: 6-31356381-GC-G
• MyVariant Identifiers: chr6:g.31324159del (hg19) ; chr6:g.31356382del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356382del , CM000668.2:g.31356382del	GRCh38
NC_000006.11:g.31324159del , CM000668.1:g.31324159del	GRCh37
NC_000006.10:g.31432138del	NCBI36
NG_023187.1:g.5831del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1877del
ENST00000481849.6:n.1877del
ENST00000497377.6:n.1877del
ENST00000640094.2:c.404del	ENSP00000491275.2:p.Arg135ProfsTer16
ENST00000696558.1:c.404del	ENSP00000512716.1:p.Arg135ProfsTer16
ENST00000696559.1:c.404del	ENSP00000512717.1:p.Arg135ProfsTer16
ENST00000696560.1:c.404del	ENSP00000512718.1:p.Arg135ProfsTer16
ENST00000696561.1:c.404del	ENSP00000512719.1:p.Arg135ProfsTer16
ENST00000696562.1:c.404del	ENSP00000512720.1:p.Arg135ProfsTer16
ENST00000412585.7:c.404del MANE Select	ENSP00000399168.2:p.Arg135ProfsTer16
ENST00000412585.6:c.404del	ENSP00000399168.2:p.Arg135ProfsTer16
ENST00000434333.1:c.437del	ENSP00000405931.1:p.Arg146ProfsTer16
ENST00000474381.1:n.279del
ENST00000498007.1:n.670del
NM_005514.6:c.404del	NP_005505.2:p.Arg135ProfsTer16
XM_011514556.1:c.437del	XP_011512858.1:p.Arg146ProfsTer16
XM_011514557.1:c.404del	XP_011512859.1:p.Arg135ProfsTer16
XR_926175.1:n.414del
NM_005514.7:c.404del	NP_005505.2:p.Arg135ProfsTer16
NM_005514.8:c.404del MANE Select	NP_005505.2:p.Arg135ProfsTer16