Canonical Allele Identifier: CA2677957670
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356748_31356752del , CM000668.2:g.31356748_31356752del GRCh38
NC_000006.11:g.31324525_31324529del , CM000668.1:g.31324525_31324529del GRCh37
NC_000006.10:g.31432504_31432508del NCBI36
NG_023187.1:g.5462_5466del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1753_1757del
ENST00000481849.6:n.1753_1757del
ENST00000497377.6:n.1753_1757del
ENST00000640094.2:c.280_284del ENSP00000491275.2:p.Gln94ThrfsTer3
ENST00000696558.1:c.280_284del ENSP00000512716.1:p.Gln94ThrfsTer3
ENST00000696559.1:c.280_284del ENSP00000512717.1:p.Gln94ThrfsTer3
ENST00000696560.1:c.280_284del ENSP00000512718.1:p.Gln94ThrfsTer3
ENST00000696561.1:c.280_284del ENSP00000512719.1:p.Gln94ThrfsTer3
ENST00000696562.1:c.280_284del ENSP00000512720.1:p.Gln94ThrfsTer3
ENST00000412585.7:c.280_284del MANE Select ENSP00000399168.2:p.Gln94ThrfsTer3
ENST00000412585.6:c.280_284del ENSP00000399168.2:p.Gln94ThrfsTer3
ENST00000434333.1:c.313_317del ENSP00000405931.1:p.Gln105ThrfsTer3
ENST00000474381.1:n.155_159del
ENST00000498007.1:n.301_305del
ENST00000603274.1:n.102_106del
NM_005514.6:c.280_284del NP_005505.2:p.Gln94ThrfsTer3
XM_011514556.1:c.313_317del XP_011512858.1:p.Gln105ThrfsTer3
XM_011514557.1:c.280_284del XP_011512859.1:p.Gln94ThrfsTer3
XR_926175.1:n.290_294del
NM_005514.7:c.280_284del NP_005505.2:p.Gln94ThrfsTer3
NM_005514.8:c.280_284del MANE Select NP_005505.2:p.Gln94ThrfsTer3