Canonical Allele Identifier: CA136833992

Gene: HLA-B

Linked Data

• dbSNP Id: rs41543519
• gnomAD v4: 6-31356253-TC-T
• MyVariant Identifiers: chr6:g.31324031del (hg19) ; chr6:g.31356254del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356255del , CM000668.2:g.31356255del	GRCh38
NC_000006.11:g.31324032del , CM000668.1:g.31324032del	GRCh37
NC_000006.10:g.31432011del	NCBI36
NG_023187.1:g.5959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2005del
ENST00000481849.6:n.2005del
ENST00000497377.6:n.2005del
ENST00000640094.2:c.532del	ENSP00000491275.2:p.Glu178SerfsTer?
ENST00000696558.1:c.532del	ENSP00000512716.1:p.Glu178SerfsTer?
ENST00000696559.1:c.532del	ENSP00000512717.1:p.Glu178SerfsTer?
ENST00000696560.1:c.532del	ENSP00000512718.1:p.Glu178SerfsTer?
ENST00000696561.1:c.532del	ENSP00000512719.1:p.Glu178SerfsTer?
ENST00000696562.1:c.532del	ENSP00000512720.1:p.Glu178SerfsTer?
ENST00000412585.7:c.532del MANE Select	ENSP00000399168.2:p.Glu178SerfsTer?
ENST00000412585.6:c.532del	ENSP00000399168.2:p.Glu178SerfsTer?
ENST00000434333.1:c.565del	ENSP00000405931.1:p.Glu189SerfsTer?
ENST00000474381.1:n.407del
ENST00000498007.1:n.798del
NM_005514.6:c.532del	NP_005505.2:p.Glu178SerfsTer?
XM_011514556.1:c.565del	XP_011512858.1:p.Glu189SerfsTer?
XM_011514557.1:c.532del	XP_011512859.1:p.Glu178SerfsTer?
XR_926175.1:n.542del
NM_005514.7:c.532del	NP_005505.2:p.Glu178SerfsTer?
NM_005514.8:c.532del MANE Select	NP_005505.2:p.Glu178SerfsTer?