Canonical Allele Identifier: CA2677955094
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355197_31355200del , CM000668.2:g.31355197_31355200del GRCh38
NC_000006.11:g.31322974_31322977del , CM000668.1:g.31322974_31322977del GRCh37
NC_000006.10:g.31430953_31430956del NCBI36
NG_023187.1:g.7013_7016del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2966_2969del
ENST00000481849.6:n.2485_2488del
ENST00000497377.6:n.2392_2395del
ENST00000640094.2:c.895+117_895+120del ENSP00000491275.2:n.895+117_895+120del
ENST00000696558.1:c.988_991del ENSP00000512716.1:n.988_991del
ENST00000696559.1:c.919_922del ENSP00000512717.1:p.Pro307SerfsTer11
ENST00000696560.1:c.919_922del ENSP00000512718.1:p.Pro307SerfsTer11
ENST00000696561.1:c.919_922del ENSP00000512719.1:p.Pro307SerfsTer11
ENST00000696562.1:c.919_922del ENSP00000512720.1:p.Pro307SerfsTer11
ENST00000412585.7:c.919_922del MANE Select ENSP00000399168.2:p.Pro307SerfsTer11
ENST00000640094.1:c.88+117_88+120del ENSP00000491275.1:n.88+117_88+120del
ENST00000412585.6:c.919_922del ENSP00000399168.2:p.Pro307SerfsTer11
ENST00000463574.1:n.510_513del
NM_005514.6:c.919_922del NP_005505.2:p.Pro307SerfsTer11
XM_011514556.1:c.952_955del XP_011512858.1:p.Pro318SerfsTer11
XM_011514557.1:c.895+117_895+120del XP_011512859.1:n.895+117_895+120del
XR_926175.1:n.1358_1361del
NM_005514.7:c.919_922del NP_005505.2:p.Pro307SerfsTer11
NM_005514.8:c.919_922del MANE Select NP_005505.2:p.Pro307SerfsTer11