Canonical Allele Identifier: CA377334079

Gene: POLR3A

Linked Data

• dbSNP Id: rs1847266906
• MyVariant Identifiers: chr10:g.79753003C>G (hg19) ; chr10:g.77993245C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993245C>G , CM000672.2:g.77993245C>G	GRCh38
NC_000010.10:g.79753003C>G , CM000672.1:g.79753003C>G	GRCh37
NC_000010.9:g.79423009C>G	NCBI36
NG_029648.1:g.41296G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.7G>C
ENST00000698727.1:n.1799G>C
ENST00000698728.1:n.2318G>C
ENST00000698729.1:n.3864G>C
ENST00000698730.1:n.3864G>C
ENST00000698731.1:c.2598G>C	ENSP00000513898.1:p.Glu866Asp
ENST00000698732.1:c.*1600G>C	ENSP00000513899.1:n.*1600G>C
ENST00000698733.1:c.*1926G>C	ENSP00000513900.1:n.*1926G>C
ENST00000698734.1:c.*263G>C	ENSP00000513901.1:n.*263G>C
ENST00000698735.1:n.2854G>C
ENST00000698736.1:n.2854G>C
ENST00000698737.1:n.2854G>C
ENST00000698738.1:n.2854G>C
ENST00000698739.1:n.2854G>C
ENST00000372371.8:c.2739G>C MANE Select	ENSP00000361446.3:p.Glu913Asp
ENST00000372371.7:c.2739G>C	ENSP00000361446.3:p.Glu913Asp
ENST00000472014.5:n.592G>C
NM_007055.3:c.2739G>C	NP_008986.2:p.Glu913Asp
NM_007055.4:c.2739G>C MANE Select	NP_008986.2:p.Glu913Asp