Canonical Allele Identifier: CA210186590

Gene: POLR3A

Linked Data

• dbSNP Id: rs559554208
• gnomAD v3: 10-77980233-A-G
• gnomAD v4: 10-77980233-A-G
• MyVariant Identifiers: chr10:g.79739991A>G (hg19) ; chr10:g.77980233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980233A>G , CM000672.2:g.77980233A>G	GRCh38
NC_000010.10:g.79739991A>G , CM000672.1:g.79739991A>G	GRCh37
NC_000010.9:g.79409997A>G	NCBI36
NG_029648.1:g.54308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1849T>C
ENST00000698725.1:n.1602T>C
ENST00000698726.1:n.3162T>C
ENST00000698727.1:n.2895T>C
ENST00000698728.1:n.3511T>C
ENST00000698729.1:n.4959T>C
ENST00000698730.1:n.5057T>C
ENST00000698731.1:c.3791T>C	ENSP00000513898.1:p.Met1264Thr
ENST00000698732.1:c.*2621T>C	ENSP00000513899.1:n.*2621T>C
ENST00000698733.1:c.*3119T>C	ENSP00000513900.1:n.*3119T>C
ENST00000698734.1:c.*2105T>C	ENSP00000513901.1:n.*2105T>C
ENST00000698735.1:n.4283T>C
ENST00000698736.1:n.4696T>C
ENST00000698737.1:n.4047T>C
ENST00000372371.8:c.3932T>C MANE Select	ENSP00000361446.3:p.Met1311Thr
ENST00000372371.7:c.3932T>C	ENSP00000361446.3:p.Met1311Thr
ENST00000616246.4:c.380T>C	ENSP00000483738.1:p.Met127Thr
NM_007055.3:c.3932T>C	NP_008986.2:p.Met1311Thr
NM_007055.4:c.3932T>C MANE Select	NP_008986.2:p.Met1311Thr