Canonical Allele Identifier: CA2677956962

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356435-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356435_31356436insA , CM000668.2:g.31356435_31356436insA	GRCh38
NC_000006.11:g.31324212_31324213insA , CM000668.1:g.31324212_31324213insA	GRCh37
NC_000006.10:g.31432191_31432192insA	NCBI36
NG_023187.1:g.5777_5778insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1823_1824insT
ENST00000481849.6:n.1823_1824insT
ENST00000497377.6:n.1823_1824insT
ENST00000640094.2:c.350_351insT	ENSP00000491275.2:p.Thr118HisfsTer21
ENST00000696558.1:c.350_351insT	ENSP00000512716.1:p.Thr118HisfsTer21
ENST00000696559.1:c.350_351insT	ENSP00000512717.1:p.Thr118HisfsTer21
ENST00000696560.1:c.350_351insT	ENSP00000512718.1:p.Thr118HisfsTer21
ENST00000696561.1:c.350_351insT	ENSP00000512719.1:p.Thr118HisfsTer21
ENST00000696562.1:c.350_351insT	ENSP00000512720.1:p.Thr118HisfsTer21
ENST00000412585.7:c.350_351insT MANE Select	ENSP00000399168.2:p.Thr118HisfsTer21
ENST00000412585.6:c.350_351insT	ENSP00000399168.2:p.Thr118HisfsTer21
ENST00000434333.1:c.383_384insT	ENSP00000405931.1:p.Thr129HisfsTer21
ENST00000474381.1:n.225_226insT
ENST00000498007.1:n.616_617insT
NM_005514.6:c.350_351insT	NP_005505.2:p.Thr118HisfsTer21
XM_011514556.1:c.383_384insT	XP_011512858.1:p.Thr129HisfsTer21
XM_011514557.1:c.350_351insT	XP_011512859.1:p.Thr118HisfsTer21
XR_926175.1:n.360_361insT
NM_005514.7:c.350_351insT	NP_005505.2:p.Thr118HisfsTer21
NM_005514.8:c.350_351insT MANE Select	NP_005505.2:p.Thr118HisfsTer21