Canonical Allele Identifier: CA470397164

Gene: POLR3A

Linked Data

• dbSNP Id: rs1255734863
• gnomAD v2: 10-79759802-T-C
• gnomAD v4: 10-78000044-T-C
• MyVariant Identifiers: chr10:g.79759802T>C (hg19) ; chr10:g.78000044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78000044T>C , CM000672.2:g.78000044T>C	GRCh38
NC_000010.10:g.79759802T>C , CM000672.1:g.79759802T>C	GRCh37
NC_000010.9:g.79429808T>C	NCBI36
NG_029648.1:g.34497A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1613A>G
ENST00000698728.1:n.2132A>G
ENST00000698729.1:n.3678A>G
ENST00000698730.1:n.3678A>G
ENST00000698731.1:c.2412A>G	ENSP00000513898.1:p.Thr804=
ENST00000698732.1:c.*1414A>G	ENSP00000513899.1:n.*1414A>G
ENST00000698733.1:c.*1740A>G	ENSP00000513900.1:n.*1740A>G
ENST00000698734.1:c.2553A>G	ENSP00000513901.1:p.Thr851=
ENST00000698735.1:n.2668A>G
ENST00000698736.1:n.2668A>G
ENST00000698737.1:n.2668A>G
ENST00000698738.1:n.2668A>G
ENST00000698739.1:n.2668A>G
ENST00000372371.8:c.2553A>G MANE Select	ENSP00000361446.3:p.Thr851=
ENST00000372371.7:c.2553A>G	ENSP00000361446.3:p.Thr851=
ENST00000472014.5:n.469+4672A>G
NM_007055.3:c.2553A>G	NP_008986.2:p.Thr851=
NM_007055.4:c.2553A>G MANE Select	NP_008986.2:p.Thr851=