Canonical Allele Identifier: CA2677955076
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355174_31355182del , CM000668.2:g.31355174_31355182del GRCh38
NC_000006.11:g.31322951_31322959del , CM000668.1:g.31322951_31322959del GRCh37
NC_000006.10:g.31430930_31430938del NCBI36
NG_023187.1:g.7035_7043del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2988_2996del
ENST00000481849.6:n.2507_2515del
ENST00000497377.6:n.2414_2422del
ENST00000640094.2:c.895+139_895+147del ENSP00000491275.2:n.895+139_895+147del
ENST00000696558.1:c.1010_1018del ENSP00000512716.1:n.1010_1018del
ENST00000696559.1:c.941_949del ENSP00000512717.1:p.Gly314_Ala316del
ENST00000696560.1:c.941_949del ENSP00000512718.1:p.Gly314_Ala316del
ENST00000696561.1:c.941_949del ENSP00000512719.1:p.Gly314_Ala316del
ENST00000696562.1:c.941_949del ENSP00000512720.1:p.Gly314_Ala316del
ENST00000412585.7:c.941_949del MANE Select ENSP00000399168.2:p.Gly314_Ala316del
ENST00000640094.1:c.88+139_88+147del ENSP00000491275.1:n.88+139_88+147del
ENST00000412585.6:c.941_949del ENSP00000399168.2:p.Gly314_Ala316del
ENST00000463574.1:n.532_540del
NM_005514.6:c.941_949del NP_005505.2:p.Gly314_Ala316del
XM_011514556.1:c.974_982del XP_011512858.1:p.Gly325_Ala327del
XM_011514557.1:c.895+139_895+147del XP_011512859.1:n.895+139_895+147del
XR_926175.1:n.1380_1388del
NM_005514.7:c.941_949del NP_005505.2:p.Gly314_Ala316del
NM_005514.8:c.941_949del MANE Select NP_005505.2:p.Gly314_Ala316del