Canonical Allele Identifier: CA470398294
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79769646G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009888G>T , CM000672.2:g.78009888G>T GRCh38
NC_000010.10:g.79769646G>T , CM000672.1:g.79769646G>T GRCh37
NC_000010.9:g.79439652G>T NCBI36
NG_029648.1:g.24653C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698728.1:n.1325C>A
ENST00000698729.1:n.2871C>A
ENST00000698730.1:n.2871C>A
ENST00000698731.1:c.1605C>A ENSP00000513898.1:p.Arg535=
ENST00000698732.1:c.*607C>A ENSP00000513899.1:n.*607C>A
ENST00000698733.1:c.*933C>A ENSP00000513900.1:n.*933C>A
ENST00000698734.1:c.1746C>A ENSP00000513901.1:p.Arg582=
ENST00000698735.1:n.1861C>A
ENST00000698736.1:n.1861C>A
ENST00000698737.1:n.1861C>A
ENST00000698738.1:n.1861C>A
ENST00000698739.1:n.1861C>A
ENST00000372371.8:c.1746C>A MANE Select ENSP00000361446.3:p.Arg582=
ENST00000372371.7:c.1746C>A ENSP00000361446.3:p.Arg582=
ENST00000473588.2:c.548C>A
NM_007055.3:c.1746C>A NP_008986.2:p.Arg582=
NM_007055.4:c.1746C>A MANE Select NP_008986.2:p.Arg582=