Canonical Allele Identifier: CA2677957396
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356532_31356533insGGCC , CM000668.2:g.31356532_31356533insGGCC GRCh38
NC_000006.11:g.31324309_31324310insGGCC , CM000668.1:g.31324309_31324310insGGCC GRCh37
NC_000006.10:g.31432288_31432289insGGCC NCBI36
NG_023187.1:g.5680_5681insGGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-91_1817-90insGGCC
ENST00000481849.6:n.1817-91_1817-90insGGCC
ENST00000497377.6:n.1817-91_1817-90insGGCC
ENST00000640094.2:c.344-91_344-90insGGCC ENSP00000491275.2:n.344-91_344-90insGGCC
ENST00000696558.1:c.344-91_344-90insGGCC ENSP00000512716.1:n.344-91_344-90insGGCC
ENST00000696559.1:c.344-91_344-90insGGCC ENSP00000512717.1:n.344-91_344-90insGGCC
ENST00000696560.1:c.344-91_344-90insGGCC ENSP00000512718.1:n.344-91_344-90insGGCC
ENST00000696561.1:c.344-91_344-90insGGCC ENSP00000512719.1:n.344-91_344-90insGGCC
ENST00000696562.1:c.344-91_344-90insGGCC ENSP00000512720.1:n.344-91_344-90insGGCC
ENST00000412585.7:c.344-91_344-90insGGCC MANE Select ENSP00000399168.2:n.344-91_344-90insGGCC
ENST00000412585.6:c.344-91_344-90insGGCC ENSP00000399168.2:n.344-91_344-90insGGCC
ENST00000434333.1:c.377-91_377-90insGGCC ENSP00000405931.1:n.377-91_377-90insGGCC
ENST00000474381.1:n.219-91_219-90insGGCC
ENST00000498007.1:n.519_520insGGCC
NM_005514.6:c.344-91_344-90insGGCC NP_005505.2:n.344-91_344-90insGGCC
XM_011514556.1:c.377-91_377-90insGGCC XP_011512858.1:n.377-91_377-90insGGCC
XM_011514557.1:c.344-91_344-90insGGCC XP_011512859.1:n.344-91_344-90insGGCC
XR_926175.1:n.354-91_354-90insGGCC
NM_005514.7:c.344-91_344-90insGGCC NP_005505.2:n.344-91_344-90insGGCC
NM_005514.8:c.344-91_344-90insGGCC MANE Select NP_005505.2:n.344-91_344-90insGGCC