Canonical Allele Identifier: CA1921508749

Gene: POLR3A

Linked Data

• dbSNP Id: rs1847396505

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004933C>G , CM000672.2:g.78004933C>G	GRCh38
NC_000010.10:g.79764691C>G , CM000672.1:g.79764691C>G	GRCh37
NC_000010.9:g.79434697C>G	NCBI36
NG_029648.1:g.29608G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1135-45G>C
ENST00000698728.1:n.1654-45G>C
ENST00000698729.1:n.3200-45G>C
ENST00000698730.1:n.3200-45G>C
ENST00000698731.1:c.1934-45G>C	ENSP00000513898.1:n.1934-45G>C
ENST00000698732.1:c.*936-45G>C	ENSP00000513899.1:n.*936-45G>C
ENST00000698733.1:c.*1262-45G>C	ENSP00000513900.1:n.*1262-45G>C
ENST00000698734.1:c.2075-45G>C	ENSP00000513901.1:n.2075-45G>C
ENST00000698735.1:n.2190-45G>C
ENST00000698736.1:n.2190-45G>C
ENST00000698737.1:n.2190-45G>C
ENST00000698738.1:n.2190-45G>C
ENST00000698739.1:n.2190-45G>C
ENST00000372371.8:c.2075-45G>C MANE Select	ENSP00000361446.3:n.2075-45G>C
ENST00000372371.7:c.2075-45G>C	ENSP00000361446.3:n.2075-45G>C
ENST00000472014.5:n.297-45G>C
ENST00000473588.2:c.738-45G>C
NM_007055.3:c.2075-45G>C	NP_008986.2:n.2075-45G>C
NM_007055.4:c.2075-45G>C MANE Select	NP_008986.2:n.2075-45G>C