Canonical Allele Identifier: CA136833193
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341338
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355854del , CM000668.2:g.31355854del GRCh38
NC_000006.11:g.31323631del , CM000668.1:g.31323631del GRCh37
NC_000006.10:g.31431610del NCBI36
NG_023187.1:g.6361del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2407del
ENST00000481849.6:n.2093-260del
ENST00000497377.6:n.2093-260del
ENST00000640094.2:c.620-260del ENSP00000491275.2:n.620-260del
ENST00000696558.1:c.620-46del ENSP00000512716.1:n.620-46del
ENST00000696559.1:c.620-260del ENSP00000512717.1:n.620-260del
ENST00000696560.1:c.620-260del ENSP00000512718.1:n.620-260del
ENST00000696561.1:c.620-260del ENSP00000512719.1:n.620-260del
ENST00000696562.1:c.620-260del ENSP00000512720.1:n.620-260del
ENST00000412585.7:c.620-260del MANE Select ENSP00000399168.2:n.620-260del
ENST00000412585.6:c.620-260del ENSP00000399168.2:n.620-260del
ENST00000434333.1:c.653-260del ENSP00000405931.1:n.653-260del
ENST00000474381.1:n.809del
ENST00000498007.1:n.886-260del
NM_005514.6:c.620-260del NP_005505.2:n.620-260del
XM_011514556.1:c.653-260del XP_011512858.1:n.653-260del
XM_011514557.1:c.620-260del XP_011512859.1:n.620-260del
XR_926175.1:n.944del
NM_005514.7:c.620-260del NP_005505.2:n.620-260del
NM_005514.8:c.620-260del MANE Select NP_005505.2:n.620-260del
Search 100 bp 5'
Search 100 bp 3'