Canonical Allele Identifier: CA2677956597
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356246_31356247insA , CM000668.2:g.31356246_31356247insA GRCh38
NC_000006.11:g.31324023_31324024insA , CM000668.1:g.31324023_31324024insA GRCh37
NC_000006.10:g.31432002_31432003insA NCBI36
NG_023187.1:g.5966_5967insT

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2012_2013insT
ENST00000481849.6:n.2012_2013insT
ENST00000497377.6:n.2012_2013insT
ENST00000640094.2:c.539_540insT ENSP00000491275.2:p.Arg181GlufsTer27
ENST00000696558.1:c.539_540insT ENSP00000512716.1:p.Arg181GlufsTer27
ENST00000696559.1:c.539_540insT ENSP00000512717.1:p.Arg181GlufsTer27
ENST00000696560.1:c.539_540insT ENSP00000512718.1:p.Arg181GlufsTer27
ENST00000696561.1:c.539_540insT ENSP00000512719.1:p.Arg181GlufsTer27
ENST00000696562.1:c.539_540insT ENSP00000512720.1:p.Arg181GlufsTer27
ENST00000412585.7:c.539_540insT MANE Select ENSP00000399168.2:p.Arg181GlufsTer27
ENST00000412585.6:c.539_540insT ENSP00000399168.2:p.Arg181GlufsTer27
ENST00000434333.1:c.572_573insT ENSP00000405931.1:p.Arg192GlufsTer27
ENST00000474381.1:n.414_415insT
ENST00000498007.1:n.805_806insT
NM_005514.6:c.539_540insT NP_005505.2:p.Arg181GlufsTer27
XM_011514556.1:c.572_573insT XP_011512858.1:p.Arg192GlufsTer27
XM_011514557.1:c.539_540insT XP_011512859.1:p.Arg181GlufsTer27
XR_926175.1:n.549_550insT
NM_005514.7:c.539_540insT NP_005505.2:p.Arg181GlufsTer27
NM_005514.8:c.539_540insT MANE Select NP_005505.2:p.Arg181GlufsTer27