Canonical Allele Identifier: CA2677955089
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355187_31355199del , CM000668.2:g.31355187_31355199del GRCh38
NC_000006.11:g.31322964_31322976del , CM000668.1:g.31322964_31322976del GRCh37
NC_000006.10:g.31430943_31430955del NCBI36
NG_023187.1:g.7014_7026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2967_2979del
ENST00000481849.6:n.2486_2498del
ENST00000497377.6:n.2393_2405del
ENST00000640094.2:c.895+118_895+130del ENSP00000491275.2:n.895+118_895+130del
ENST00000696558.1:c.989_1001del ENSP00000512716.1:n.989_1001del
ENST00000696559.1:c.920_932del ENSP00000512717.1:p.Pro307LeufsTer8
ENST00000696560.1:c.920_932del ENSP00000512718.1:p.Pro307LeufsTer8
ENST00000696561.1:c.920_932del ENSP00000512719.1:p.Pro307LeufsTer8
ENST00000696562.1:c.920_932del ENSP00000512720.1:p.Pro307LeufsTer8
ENST00000412585.7:c.920_932del MANE Select ENSP00000399168.2:p.Pro307LeufsTer8
ENST00000640094.1:c.88+118_88+130del ENSP00000491275.1:n.88+118_88+130del
ENST00000412585.6:c.920_932del ENSP00000399168.2:p.Pro307LeufsTer8
ENST00000463574.1:n.511_523del
NM_005514.6:c.920_932del NP_005505.2:p.Pro307LeufsTer8
XM_011514556.1:c.953_965del XP_011512858.1:p.Pro318LeufsTer8
XM_011514557.1:c.895+118_895+130del XP_011512859.1:n.895+118_895+130del
XR_926175.1:n.1359_1371del
NM_005514.7:c.920_932del NP_005505.2:p.Pro307LeufsTer8
NM_005514.8:c.920_932del MANE Select NP_005505.2:p.Pro307LeufsTer8