Canonical Allele Identifier: CA2677954934
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355126_31355127del , CM000668.2:g.31355126_31355127del GRCh38
NC_000006.11:g.31322903_31322904del , CM000668.1:g.31322903_31322904del GRCh37
NC_000006.10:g.31430882_31430883del NCBI36
NG_023187.1:g.7089_7090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3042_3043del
ENST00000481849.6:n.2561_2562del
ENST00000497377.6:n.2468_2469del
ENST00000640094.2:c.895+193_895+194del ENSP00000491275.2:n.895+193_895+194del
ENST00000696558.1:c.1064_1065del ENSP00000512716.1:n.1064_1065del
ENST00000696559.1:c.995_996del ENSP00000512717.1:p.Cys332Ter
ENST00000696560.1:c.995_996del ENSP00000512718.1:p.Cys332Ter
ENST00000696561.1:c.995_996del ENSP00000512719.1:p.Cys332Ter
ENST00000696562.1:c.995_996del ENSP00000512720.1:p.Cys332Ter
ENST00000412585.7:c.995_996del MANE Select ENSP00000399168.2:p.Cys332Ter
ENST00000640094.1:c.88+193_88+194del ENSP00000491275.1:n.88+193_88+194del
ENST00000412585.6:c.995_996del ENSP00000399168.2:p.Cys332Ter
ENST00000463574.1:n.586_587del
NM_005514.6:c.995_996del NP_005505.2:p.Cys332Ter
XM_011514556.1:c.1028_1029del XP_011512858.1:p.Cys343Ter
XM_011514557.1:c.895+193_895+194del XP_011512859.1:n.895+193_895+194del
XR_926175.1:n.1434_1435del
NM_005514.7:c.995_996del NP_005505.2:p.Cys332Ter
NM_005514.8:c.995_996del MANE Select NP_005505.2:p.Cys332Ter