Canonical Allele Identifier: CA470398289
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79769640T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009882T>C , CM000672.2:g.78009882T>C GRCh38
NC_000010.10:g.79769640T>C , CM000672.1:g.79769640T>C GRCh37
NC_000010.9:g.79439646T>C NCBI36
NG_029648.1:g.24659A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698728.1:n.1331A>G
ENST00000698729.1:n.2877A>G
ENST00000698730.1:n.2877A>G
ENST00000698731.1:c.1611A>G ENSP00000513898.1:p.Pro537=
ENST00000698732.1:c.*613A>G ENSP00000513899.1:n.*613A>G
ENST00000698733.1:c.*939A>G ENSP00000513900.1:n.*939A>G
ENST00000698734.1:c.1752A>G ENSP00000513901.1:p.Pro584=
ENST00000698735.1:n.1867A>G
ENST00000698736.1:n.1867A>G
ENST00000698737.1:n.1867A>G
ENST00000698738.1:n.1867A>G
ENST00000698739.1:n.1867A>G
ENST00000372371.8:c.1752A>G MANE Select ENSP00000361446.3:p.Pro584=
ENST00000372371.7:c.1752A>G ENSP00000361446.3:p.Pro584=
ENST00000473588.2:c.554A>G
NM_007055.3:c.1752A>G NP_008986.2:p.Pro584=
NM_007055.4:c.1752A>G MANE Select NP_008986.2:p.Pro584=