Canonical Allele Identifier: CA2677955336
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355560del , CM000668.2:g.31355560del GRCh38
NC_000006.11:g.31323337del , CM000668.1:g.31323337del GRCh37
NC_000006.10:g.31431316del NCBI36
NG_023187.1:g.6653del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2699del
ENST00000481849.6:n.2125del
ENST00000497377.6:n.2125del
ENST00000640094.2:c.652del ENSP00000491275.2:p.Ile218SerfsTer8
ENST00000696558.1:c.721del ENSP00000512716.1:n.721del
ENST00000696559.1:c.652del ENSP00000512717.1:p.Ile218SerfsTer8
ENST00000696560.1:c.652del ENSP00000512718.1:p.Ile218SerfsTer8
ENST00000696561.1:c.652del ENSP00000512719.1:p.Ile218SerfsTer8
ENST00000696562.1:c.652del ENSP00000512720.1:p.Ile218SerfsTer8
ENST00000412585.7:c.652del MANE Select ENSP00000399168.2:p.Ile218SerfsTer8
ENST00000412585.6:c.652del ENSP00000399168.2:p.Ile218SerfsTer8
ENST00000434333.1:c.685del ENSP00000405931.1:p.Ile229SerfsTer8
ENST00000463574.1:n.243del
ENST00000474381.1:n.1101del
ENST00000498007.1:n.918del
NM_005514.6:c.652del NP_005505.2:p.Ile218SerfsTer8
XM_011514556.1:c.685del XP_011512858.1:p.Ile229SerfsTer8
XM_011514557.1:c.652del XP_011512859.1:p.Ile218SerfsTer8
XR_926175.1:n.1091del
NM_005514.7:c.652del NP_005505.2:p.Ile218SerfsTer8
NM_005514.8:c.652del MANE Select NP_005505.2:p.Ile218SerfsTer8