Canonical Allele Identifier: CA470394810

Gene: POLR3A

Linked Data

• dbSNP Id: rs1171129827
• gnomAD v2: 10-79752991-T-C
• gnomAD v4: 10-77993233-T-C
• MyVariant Identifiers: chr10:g.79752991T>C (hg19) ; chr10:g.77993233T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993233T>C , CM000672.2:g.77993233T>C	GRCh38
NC_000010.10:g.79752991T>C , CM000672.1:g.79752991T>C	GRCh37
NC_000010.9:g.79422997T>C	NCBI36
NG_029648.1:g.41308A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.19A>G
ENST00000698727.1:n.1811A>G
ENST00000698728.1:n.2330A>G
ENST00000698729.1:n.3876A>G
ENST00000698730.1:n.3876A>G
ENST00000698731.1:c.2610A>G	ENSP00000513898.1:p.Glu870=
ENST00000698732.1:c.*1612A>G	ENSP00000513899.1:n.*1612A>G
ENST00000698733.1:c.*1938A>G	ENSP00000513900.1:n.*1938A>G
ENST00000698734.1:c.*275A>G	ENSP00000513901.1:n.*275A>G
ENST00000698735.1:n.2866A>G
ENST00000698736.1:n.2866A>G
ENST00000698737.1:n.2866A>G
ENST00000698738.1:n.2866A>G
ENST00000698739.1:n.2866A>G
ENST00000372371.8:c.2751A>G MANE Select	ENSP00000361446.3:p.Glu917=
ENST00000372371.7:c.2751A>G	ENSP00000361446.3:p.Glu917=
ENST00000472014.5:n.604A>G
NM_007055.3:c.2751A>G	NP_008986.2:p.Glu917=
NM_007055.4:c.2751A>G MANE Select	NP_008986.2:p.Glu917=