Canonical Allele Identifier: CA566689126

Gene: HLA-B

Linked Data

• dbSNP Id: rs1562163978
• gnomAD v2: 6-31323125-CT-C
• gnomAD v4: 6-31355348-CT-C
• MyVariant Identifiers: chr6:g.31323126del (hg19) ; chr6:g.31355349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355349del , CM000668.2:g.31355349del	GRCh38
NC_000006.11:g.31323126del , CM000668.1:g.31323126del	GRCh37
NC_000006.10:g.31431105del	NCBI36
NG_023187.1:g.6864del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2910del
ENST00000481849.6:n.2336del
ENST00000497377.6:n.2336del
ENST00000640094.2:c.863del	ENSP00000491275.2:p.Glu288GlyfsTer9
ENST00000696558.1:c.932del	ENSP00000512716.1:n.932del
ENST00000696559.1:c.863del	ENSP00000512717.1:p.Glu288GlyfsTer9
ENST00000696560.1:c.863del	ENSP00000512718.1:p.Glu288GlyfsTer9
ENST00000696561.1:c.863del	ENSP00000512719.1:p.Glu288GlyfsTer9
ENST00000696562.1:c.863del	ENSP00000512720.1:p.Glu288GlyfsTer9
ENST00000412585.7:c.863del MANE Select	ENSP00000399168.2:p.Glu288GlyfsTer9
ENST00000640094.1:c.56del	ENSP00000491275.1:p.Glu19GlyfsTer9
ENST00000412585.6:c.863del	ENSP00000399168.2:p.Glu288GlyfsTer9
ENST00000463574.1:n.454del
NM_005514.6:c.863del	NP_005505.2:p.Glu288GlyfsTer9
XM_011514556.1:c.896del	XP_011512858.1:p.Glu299GlyfsTer9
XM_011514557.1:c.863del	XP_011512859.1:p.Glu288GlyfsTer9
XR_926175.1:n.1302del
NM_005514.7:c.863del	NP_005505.2:p.Glu288GlyfsTer9
NM_005514.8:c.863del MANE Select	NP_005505.2:p.Glu288GlyfsTer9