Canonical Allele Identifier: CA2677957126
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356467_31356468del , CM000668.2:g.31356467_31356468del GRCh38
NC_000006.11:g.31324244_31324245del , CM000668.1:g.31324244_31324245del GRCh37
NC_000006.10:g.31432223_31432224del NCBI36
NG_023187.1:g.5745_5746del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-26_1817-25del
ENST00000481849.6:n.1817-26_1817-25del
ENST00000497377.6:n.1817-26_1817-25del
ENST00000640094.2:c.344-26_344-25del ENSP00000491275.2:n.344-26_344-25del
ENST00000696558.1:c.344-26_344-25del ENSP00000512716.1:n.344-26_344-25del
ENST00000696559.1:c.344-26_344-25del ENSP00000512717.1:n.344-26_344-25del
ENST00000696560.1:c.344-26_344-25del ENSP00000512718.1:n.344-26_344-25del
ENST00000696561.1:c.344-26_344-25del ENSP00000512719.1:n.344-26_344-25del
ENST00000696562.1:c.344-26_344-25del ENSP00000512720.1:n.344-26_344-25del
ENST00000412585.7:c.344-26_344-25del MANE Select ENSP00000399168.2:n.344-26_344-25del
ENST00000412585.6:c.344-26_344-25del ENSP00000399168.2:n.344-26_344-25del
ENST00000434333.1:c.377-26_377-25del ENSP00000405931.1:n.377-26_377-25del
ENST00000474381.1:n.219-26_219-25del
ENST00000498007.1:n.584_585del
NM_005514.6:c.344-26_344-25del NP_005505.2:n.344-26_344-25del
XM_011514556.1:c.377-26_377-25del XP_011512858.1:n.377-26_377-25del
XM_011514557.1:c.344-26_344-25del XP_011512859.1:n.344-26_344-25del
XR_926175.1:n.354-26_354-25del
NM_005514.7:c.344-26_344-25del NP_005505.2:n.344-26_344-25del
NM_005514.8:c.344-26_344-25del MANE Select NP_005505.2:n.344-26_344-25del