Canonical Allele Identifier: CA470398287
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79769637C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009879C>G , CM000672.2:g.78009879C>G GRCh38
NC_000010.10:g.79769637C>G , CM000672.1:g.79769637C>G GRCh37
NC_000010.9:g.79439643C>G NCBI36
NG_029648.1:g.24662G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698728.1:n.1334G>C
ENST00000698729.1:n.2880G>C
ENST00000698730.1:n.2880G>C
ENST00000698731.1:c.1614G>C ENSP00000513898.1:p.Pro538=
ENST00000698732.1:c.*616G>C ENSP00000513899.1:n.*616G>C
ENST00000698733.1:c.*942G>C ENSP00000513900.1:n.*942G>C
ENST00000698734.1:c.1755G>C ENSP00000513901.1:p.Pro585=
ENST00000698735.1:n.1870G>C
ENST00000698736.1:n.1870G>C
ENST00000698737.1:n.1870G>C
ENST00000698738.1:n.1870G>C
ENST00000698739.1:n.1870G>C
ENST00000372371.8:c.1755G>C MANE Select ENSP00000361446.3:p.Pro585=
ENST00000372371.7:c.1755G>C ENSP00000361446.3:p.Pro585=
ENST00000473588.2:c.557G>C
NM_007055.3:c.1755G>C NP_008986.2:p.Pro585=
NM_007055.4:c.1755G>C MANE Select NP_008986.2:p.Pro585=