Canonical Allele Identifier: CA1921495620

Gene: POLR3A

Linked Data

• dbSNP Id: rs1847083502
• gnomAD v4: 10-77975865-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975865A>G , CM000672.2:g.77975865A>G	GRCh38
NC_000010.10:g.79735623A>G , CM000672.1:g.79735623A>G	GRCh37
NC_000010.9:g.79405629A>G	NCBI36
NG_029648.1:g.58676T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1941+4276T>C
ENST00000698725.1:n.3456T>C
ENST00000698726.1:n.5016T>C
ENST00000698727.1:n.4749T>C
ENST00000698728.1:n.5365T>C
ENST00000698729.1:n.6813T>C
ENST00000698730.1:n.6911T>C
ENST00000698731.1:c.*1613T>C	ENSP00000513898.1:n.*1613T>C
ENST00000698732.1:c.*4475T>C	ENSP00000513899.1:n.*4475T>C
ENST00000698733.1:c.*4973T>C	ENSP00000513900.1:n.*4973T>C
ENST00000698734.1:c.*3959T>C	ENSP00000513901.1:n.*3959T>C
ENST00000698735.1:n.6137T>C
ENST00000698736.1:n.6550T>C
ENST00000372371.8:c.*1613T>C MANE Select	ENSP00000361446.3:n.*1613T>C
ENST00000372371.7:c.*1613T>C	ENSP00000361446.3:n.*1613T>C
ENST00000616246.4:c.472+4276T>C	ENSP00000483738.1:n.472+4276T>C
NM_007055.3:c.*1613T>C	NP_008986.2:n.*1613T>C
NM_007055.4:c.*1613T>C MANE Select	NP_008986.2:n.*1613T>C