Canonical Allele Identifier: CA668632919

Gene: POLR3A

Linked Data

• dbSNP Id: rs909567042
• gnomAD v3: 10-77975810-G-T
• gnomAD v4: 10-77975810-G-T
• MyVariant Identifiers: chr10:g.79735568G>T (hg19) ; chr10:g.77975810G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975810G>T , CM000672.2:g.77975810G>T	GRCh38
NC_000010.10:g.79735568G>T , CM000672.1:g.79735568G>T	GRCh37
NC_000010.9:g.79405574G>T	NCBI36
NG_029648.1:g.58731C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4331C>A
ENST00000698725.1:n.3511C>A
ENST00000698726.1:n.5071C>A
ENST00000698727.1:n.4804C>A
ENST00000698728.1:n.5420C>A
ENST00000698729.1:n.6868C>A
ENST00000698730.1:n.6966C>A
ENST00000698731.1:c.*1668C>A	ENSP00000513898.1:n.*1668C>A
ENST00000698732.1:c.*4530C>A	ENSP00000513899.1:n.*4530C>A
ENST00000698733.1:c.*5028C>A	ENSP00000513900.1:n.*5028C>A
ENST00000698734.1:c.*4014C>A	ENSP00000513901.1:n.*4014C>A
ENST00000698735.1:n.6192C>A
ENST00000698736.1:n.6605C>A
ENST00000372371.8:c.*1668C>A MANE Select	ENSP00000361446.3:n.*1668C>A
ENST00000372371.7:c.*1668C>A	ENSP00000361446.3:n.*1668C>A
ENST00000616246.4:c.472+4331C>A	ENSP00000483738.1:n.472+4331C>A
NM_007055.3:c.*1668C>A	NP_008986.2:n.*1668C>A
NM_007055.4:c.*1668C>A MANE Select	NP_008986.2:n.*1668C>A