Canonical Allele Identifier: CA470397141

Gene: POLR3A

Linked Data

• gnomAD v4: 10-78000032-C-G
• MyVariant Identifiers: chr10:g.79759790C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000032C>G , CM000672.2:g.78000032C>G	GRCh38
NC_000010.10:g.79759790C>G , CM000672.1:g.79759790C>G	GRCh37
NC_000010.9:g.79429796C>G	NCBI36
NG_029648.1:g.34509G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1625G>C
ENST00000698728.1:n.2144G>C
ENST00000698729.1:n.3690G>C
ENST00000698730.1:n.3690G>C
ENST00000698731.1:c.2424G>C	ENSP00000513898.1:p.Arg808=
ENST00000698732.1:c.*1426G>C	ENSP00000513899.1:n.*1426G>C
ENST00000698733.1:c.*1752G>C	ENSP00000513900.1:n.*1752G>C
ENST00000698734.1:c.2565G>C	ENSP00000513901.1:p.Arg855=
ENST00000698735.1:n.2680G>C
ENST00000698736.1:n.2680G>C
ENST00000698737.1:n.2680G>C
ENST00000698738.1:n.2680G>C
ENST00000698739.1:n.2680G>C
ENST00000372371.8:c.2565G>C MANE Select	ENSP00000361446.3:p.Arg855=
ENST00000372371.7:c.2565G>C	ENSP00000361446.3:p.Arg855=
ENST00000472014.5:n.469+4684G>C
NM_007055.3:c.2565G>C	NP_008986.2:p.Arg855=
NM_007055.4:c.2565G>C MANE Select	NP_008986.2:p.Arg855=