Canonical Allele Identifier: CA12350804
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12528645

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355948T>C , CM000668.2:g.31355948T>C GRCh38
NC_000006.11:g.31323725T>C , CM000668.1:g.31323725T>C GRCh37
NC_000006.10:g.31431704T>C NCBI36
NG_023187.1:g.6265A>G

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.619+219A>G VV NP_005505.2:p.=
XM_011514556.1:c.652+219A>G XP_011512858.1:p.=
XM_011514557.1:c.619+219A>G XP_011512859.1:p.=
XR_926175.1:n.848A>G
NM_005514.7:c.619+219A>G VV NP_005505.2:p.=
NM_005514.8:c.619+219A>G VV MANE Preferred NP_005505.2:p.=
ENST00000412585.6:c.619+219A>G ENSP00000399168.2:p.=
ENST00000434333.1:c.652+219A>G ENSP00000405931.1:p.=
ENST00000474381.1:n.713A>G
ENST00000498007.1:n.885+219A>G