Canonical Allele Identifier: CA594426230

Gene: POLR3A

Linked Data

• dbSNP Id: rs1246309198
• gnomAD v2: 10-79740051-G-T
• MyVariant Identifiers: chr10:g.79740051G>T (hg19) ; chr10:g.77980293G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980293G>T , CM000672.2:g.77980293G>T	GRCh38
NC_000010.10:g.79740051G>T , CM000672.1:g.79740051G>T	GRCh37
NC_000010.9:g.79410057G>T	NCBI36
NG_029648.1:g.54248C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809-20C>A
ENST00000698725.1:n.1542C>A
ENST00000698726.1:n.3122-20C>A
ENST00000698727.1:n.2855-20C>A
ENST00000698728.1:n.3471-20C>A
ENST00000698729.1:n.4919-20C>A
ENST00000698730.1:n.5017-20C>A
ENST00000698731.1:c.3751-20C>A	ENSP00000513898.1:n.3751-20C>A
ENST00000698732.1:c.*2581-20C>A	ENSP00000513899.1:n.*2581-20C>A
ENST00000698733.1:c.*3079-20C>A	ENSP00000513900.1:n.*3079-20C>A
ENST00000698734.1:c.*2065-20C>A	ENSP00000513901.1:n.*2065-20C>A
ENST00000698735.1:n.4243-20C>A
ENST00000698736.1:n.4656-20C>A
ENST00000698737.1:n.4007-20C>A
ENST00000372371.8:c.3892-20C>A MANE Select	ENSP00000361446.3:n.3892-20C>A
ENST00000372371.7:c.3892-20C>A	ENSP00000361446.3:n.3892-20C>A
ENST00000616246.4:c.340-20C>A	ENSP00000483738.1:n.340-20C>A
NM_007055.3:c.3892-20C>A	NP_008986.2:n.3892-20C>A
NM_007055.4:c.3892-20C>A MANE Select	NP_008986.2:n.3892-20C>A