Canonical Allele Identifier: CA470395317

Gene: POLR3A

Linked Data

• MyVariant Identifiers: chr10:g.79753000T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993242T>G , CM000672.2:g.77993242T>G	GRCh38
NC_000010.10:g.79753000T>G , CM000672.1:g.79753000T>G	GRCh37
NC_000010.9:g.79423006T>G	NCBI36
NG_029648.1:g.41299A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.10A>C
ENST00000698727.1:n.1802A>C
ENST00000698728.1:n.2321A>C
ENST00000698729.1:n.3867A>C
ENST00000698730.1:n.3867A>C
ENST00000698731.1:c.2601A>C	ENSP00000513898.1:p.Gly867=
ENST00000698732.1:c.*1603A>C	ENSP00000513899.1:n.*1603A>C
ENST00000698733.1:c.*1929A>C	ENSP00000513900.1:n.*1929A>C
ENST00000698734.1:c.*266A>C	ENSP00000513901.1:n.*266A>C
ENST00000698735.1:n.2857A>C
ENST00000698736.1:n.2857A>C
ENST00000698737.1:n.2857A>C
ENST00000698738.1:n.2857A>C
ENST00000698739.1:n.2857A>C
ENST00000372371.8:c.2742A>C MANE Select	ENSP00000361446.3:p.Gly914=
ENST00000372371.7:c.2742A>C	ENSP00000361446.3:p.Gly914=
ENST00000472014.5:n.595A>C
NM_007055.3:c.2742A>C	NP_008986.2:p.Gly914=
NM_007055.4:c.2742A>C MANE Select	NP_008986.2:p.Gly914=