Canonical Allele Identifier: CA377334575
Gene: POLR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 427068
ClinVar RCV Id: RCV000489387
dbSNP Id: rs1085307939

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77993331G>A , CM000672.2:g.77993331G>A GRCh38
NC_000010.10:g.79753089G>A , CM000672.1:g.79753089G>A GRCh37
NC_000010.9:g.79423095G>A NCBI36
NG_029648.1:g.41210C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698727.1:n.1713C>T
ENST00000698728.1:n.2232C>T
ENST00000698729.1:n.3778C>T
ENST00000698730.1:n.3778C>T
ENST00000698731.1:c.2512C>T ENSP00000513898.1:p.Gln838Ter
ENST00000698732.1:c.*1514C>T ENSP00000513899.1:n.*1514C>T
ENST00000698733.1:c.*1840C>T ENSP00000513900.1:n.*1840C>T
ENST00000698734.1:c.*177C>T ENSP00000513901.1:n.*177C>T
ENST00000698735.1:n.2768C>T
ENST00000698736.1:n.2768C>T
ENST00000698737.1:n.2768C>T
ENST00000698738.1:n.2768C>T
ENST00000698739.1:n.2768C>T
ENST00000372371.8:c.2653C>T MANE Select ENSP00000361446.3:p.Gln885Ter
ENST00000372371.7:c.2653C>T ENSP00000361446.3:p.Gln885Ter
ENST00000472014.5:n.506C>T
NM_007055.3:c.2653C>T NP_008986.2:p.Gln885Ter
NM_007055.4:c.2653C>T MANE Select NP_008986.2:p.Gln885Ter