Canonical Allele Identifier: CA668635758

Gene: POLR3A

Linked Data

• dbSNP Id: rs1254004230
• gnomAD v3: 10-77980342-T-C
• gnomAD v4: 10-77980342-T-C
• MyVariant Identifiers: chr10:g.79740100T>C (hg19) ; chr10:g.77980342T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980342T>C , CM000672.2:g.77980342T>C	GRCh38
NC_000010.10:g.79740100T>C , CM000672.1:g.79740100T>C	GRCh37
NC_000010.9:g.79410106T>C	NCBI36
NG_029648.1:g.54199A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1809-69A>G
ENST00000698725.1:n.1493A>G
ENST00000698726.1:n.3122-69A>G
ENST00000698727.1:n.2855-69A>G
ENST00000698728.1:n.3471-69A>G
ENST00000698729.1:n.4919-69A>G
ENST00000698730.1:n.5017-69A>G
ENST00000698731.1:c.3751-69A>G	ENSP00000513898.1:n.3751-69A>G
ENST00000698732.1:c.*2581-69A>G	ENSP00000513899.1:n.*2581-69A>G
ENST00000698733.1:c.*3079-69A>G	ENSP00000513900.1:n.*3079-69A>G
ENST00000698734.1:c.*2065-69A>G	ENSP00000513901.1:n.*2065-69A>G
ENST00000698735.1:n.4243-69A>G
ENST00000698736.1:n.4656-69A>G
ENST00000698737.1:n.4007-69A>G
ENST00000372371.8:c.3892-69A>G MANE Select	ENSP00000361446.3:n.3892-69A>G
ENST00000372371.7:c.3892-69A>G	ENSP00000361446.3:n.3892-69A>G
ENST00000616246.4:c.340-69A>G	ENSP00000483738.1:n.340-69A>G
NM_007055.3:c.3892-69A>G	NP_008986.2:n.3892-69A>G
NM_007055.4:c.3892-69A>G MANE Select	NP_008986.2:n.3892-69A>G