Canonical Allele Identifier: CA343327
Gene: POLR3B HGNC NCBI

Linked Data

ClinVar Variation Id: 31164
ClinVar RCV Id: RCV000032279
dbSNP Id: rs267608683

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.106432361C>A , CM000674.2:g.106432361C>A GRCh38
NC_000012.11:g.106826139C>A , CM000674.1:g.106826139C>A GRCh37
NC_000012.10:g.105350269C>A NCBI36
NG_031837.1:g.79704C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000228347.9:c.1508C>A MANE Select ENSP00000228347.4:p.Thr503Lys
ENST00000228347.8:c.1508C>A ENSP00000228347.4:p.Thr503Lys
ENST00000539066.5:c.1334C>A ENSP00000445721.1:p.Thr445Lys
NM_001160708.1:c.1334C>A NP_001154180.1:p.Thr445Lys
NM_018082.5:c.1508C>A NP_060552.4:p.Thr503Lys
XM_017019621.2:c.1508C>A XP_016875110.1:p.Thr503Lys
NM_018082.6:c.1508C>A MANE Select NP_060552.4:p.Thr503Lys
NM_001160708.2:c.1334C>A NP_001154180.1:p.Thr445Lys