Canonical Allele Identifier: CA2677957724

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356764-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356764_31356765insA , CM000668.2:g.31356764_31356765insA	GRCh38
NC_000006.11:g.31324541_31324542insA , CM000668.1:g.31324541_31324542insA	GRCh37
NC_000006.10:g.31432520_31432521insA	NCBI36
NG_023187.1:g.5448_5449insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1739_1740insT
ENST00000481849.6:n.1739_1740insT
ENST00000497377.6:n.1739_1740insT
ENST00000640094.2:c.266_267insT	ENSP00000491275.2:p.Gln89HisfsTer10
ENST00000696558.1:c.266_267insT	ENSP00000512716.1:p.Gln89HisfsTer10
ENST00000696559.1:c.266_267insT	ENSP00000512717.1:p.Gln89HisfsTer10
ENST00000696560.1:c.266_267insT	ENSP00000512718.1:p.Gln89HisfsTer10
ENST00000696561.1:c.266_267insT	ENSP00000512719.1:p.Gln89HisfsTer10
ENST00000696562.1:c.266_267insT	ENSP00000512720.1:p.Gln89HisfsTer10
ENST00000412585.7:c.266_267insT MANE Select	ENSP00000399168.2:p.Gln89HisfsTer10
ENST00000412585.6:c.266_267insT	ENSP00000399168.2:p.Gln89HisfsTer10
ENST00000434333.1:c.299_300insT	ENSP00000405931.1:p.Gln100HisfsTer10
ENST00000474381.1:n.141_142insT
ENST00000498007.1:n.287_288insT
ENST00000603274.1:n.118_119insA
NM_005514.6:c.266_267insT	NP_005505.2:p.Gln89HisfsTer10
XM_011514556.1:c.299_300insT	XP_011512858.1:p.Gln100HisfsTer10
XM_011514557.1:c.266_267insT	XP_011512859.1:p.Gln89HisfsTer10
XR_926175.1:n.276_277insT
NM_005514.7:c.266_267insT	NP_005505.2:p.Gln89HisfsTer10
NM_005514.8:c.266_267insT MANE Select	NP_005505.2:p.Gln89HisfsTer10