Canonical Allele Identifier: CA2770503590
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355386del , CM000668.2:g.31355386del GRCh38
NC_000006.11:g.31323163del , CM000668.1:g.31323163del GRCh37
NC_000006.10:g.31431142del NCBI36
NG_023187.1:g.6828del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2874del
ENST00000481849.6:n.2300del
ENST00000497377.6:n.2300del
ENST00000640094.2:c.827del ENSP00000491275.2:p.Gly276GlufsTer21
ENST00000696558.1:c.896del ENSP00000512716.1:n.896del
ENST00000696559.1:c.827del ENSP00000512717.1:p.Gly276GlufsTer21
ENST00000696560.1:c.827del ENSP00000512718.1:p.Gly276GlufsTer21
ENST00000696561.1:c.827del ENSP00000512719.1:p.Gly276GlufsTer21
ENST00000696562.1:c.827del ENSP00000512720.1:p.Gly276GlufsTer21
ENST00000412585.7:c.827del MANE Select ENSP00000399168.2:p.Gly276GlufsTer21
ENST00000640094.1:c.20del ENSP00000491275.1:p.Gly7GlufsTer21
ENST00000412585.6:c.827del ENSP00000399168.2:p.Gly276GlufsTer21
ENST00000463574.1:n.418del
NM_005514.6:c.827del NP_005505.2:p.Gly276GlufsTer21
XM_011514556.1:c.860del XP_011512858.1:p.Gly287GlufsTer21
XM_011514557.1:c.827del XP_011512859.1:p.Gly276GlufsTer21
XR_926175.1:n.1266del
NM_005514.7:c.827del NP_005505.2:p.Gly276GlufsTer21
NM_005514.8:c.827del MANE Select NP_005505.2:p.Gly276GlufsTer21