Canonical Allele Identifier: CA470398306

Gene: POLR3A

Linked Data

• dbSNP Id: rs1847449805
• gnomAD v4: 10-78009912-G-C
• MyVariant Identifiers: chr10:g.79769670G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009912G>C , CM000672.2:g.78009912G>C	GRCh38
NC_000010.10:g.79769670G>C , CM000672.1:g.79769670G>C	GRCh37
NC_000010.9:g.79439676G>C	NCBI36
NG_029648.1:g.24629C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698728.1:n.1301C>G
ENST00000698729.1:n.2847C>G
ENST00000698730.1:n.2847C>G
ENST00000698731.1:c.1581C>G	ENSP00000513898.1:p.Gly527=
ENST00000698732.1:c.*583C>G	ENSP00000513899.1:n.*583C>G
ENST00000698733.1:c.*909C>G	ENSP00000513900.1:n.*909C>G
ENST00000698734.1:c.1722C>G	ENSP00000513901.1:p.Gly574=
ENST00000698735.1:n.1837C>G
ENST00000698736.1:n.1837C>G
ENST00000698737.1:n.1837C>G
ENST00000698738.1:n.1837C>G
ENST00000698739.1:n.1837C>G
ENST00000372371.8:c.1722C>G MANE Select	ENSP00000361446.3:p.Gly574=
ENST00000372371.7:c.1722C>G	ENSP00000361446.3:p.Gly574=
ENST00000473588.2:c.524C>G
NM_007055.3:c.1722C>G	NP_008986.2:p.Gly574=
NM_007055.4:c.1722C>G MANE Select	NP_008986.2:p.Gly574=