Canonical Allele Identifier: CA2677955481
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355716_31355729del , CM000668.2:g.31355716_31355729del GRCh38
NC_000006.11:g.31323493_31323506del , CM000668.1:g.31323493_31323506del GRCh37
NC_000006.10:g.31431472_31431485del NCBI36
NG_023187.1:g.6484_6497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2530_2543del
ENST00000481849.6:n.2093-137_2093-124del
ENST00000497377.6:n.2093-137_2093-124del
ENST00000640094.2:c.620-137_620-124del ENSP00000491275.2:n.620-137_620-124del
ENST00000696558.1:c.688+9_688+22del ENSP00000512716.1:n.688+9_688+22del
ENST00000696559.1:c.620-137_620-124del ENSP00000512717.1:n.620-137_620-124del
ENST00000696560.1:c.620-137_620-124del ENSP00000512718.1:n.620-137_620-124del
ENST00000696561.1:c.620-137_620-124del ENSP00000512719.1:n.620-137_620-124del
ENST00000696562.1:c.620-137_620-124del ENSP00000512720.1:n.620-137_620-124del
ENST00000412585.7:c.620-137_620-124del MANE Select ENSP00000399168.2:n.620-137_620-124del
ENST00000412585.6:c.620-137_620-124del ENSP00000399168.2:n.620-137_620-124del
ENST00000434333.1:c.653-137_653-124del ENSP00000405931.1:n.653-137_653-124del
ENST00000463574.1:n.74_87del
ENST00000474381.1:n.932_945del
ENST00000498007.1:n.886-137_886-124del
NM_005514.6:c.620-137_620-124del NP_005505.2:n.620-137_620-124del
XM_011514556.1:c.653-137_653-124del XP_011512858.1:n.653-137_653-124del
XM_011514557.1:c.620-137_620-124del XP_011512859.1:n.620-137_620-124del
XR_926175.1:n.1058+9_1058+22del
NM_005514.7:c.620-137_620-124del NP_005505.2:n.620-137_620-124del
NM_005514.8:c.620-137_620-124del MANE Select NP_005505.2:n.620-137_620-124del