Canonical Allele Identifier: CA136832285
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs144012689

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355003T>A , CM000668.2:g.31355003T>A GRCh38
NC_000006.11:g.31322780T>A , CM000668.1:g.31322780T>A GRCh37
NC_000006.10:g.31430759T>A NCBI36
NG_023187.1:g.7210A>T

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.1012+104A>T VV NP_005505.2:p.=
XM_011514556.1:c.1045+104A>T XP_011512858.1:p.=
XM_011514557.1:c.895+314A>T XP_011512859.1:p.=
XR_926175.1:n.1451+104A>T
NM_005514.7:c.1012+104A>T VV NP_005505.2:p.=
NM_005514.8:c.1012+104A>T VV MANE Preferred NP_005505.2:p.=
ENST00000412585.6:c.1012+104A>T ENSP00000399168.2:p.=
ENST00000497377.5:n.74A>T