Canonical Allele Identifier: CA470398275
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79769625T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009867T>C , CM000672.2:g.78009867T>C GRCh38
NC_000010.10:g.79769625T>C , CM000672.1:g.79769625T>C GRCh37
NC_000010.9:g.79439631T>C NCBI36
NG_029648.1:g.24674A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698728.1:n.1346A>G
ENST00000698729.1:n.2892A>G
ENST00000698730.1:n.2892A>G
ENST00000698731.1:c.1626A>G ENSP00000513898.1:p.Leu542=
ENST00000698732.1:c.*628A>G ENSP00000513899.1:n.*628A>G
ENST00000698733.1:c.*954A>G ENSP00000513900.1:n.*954A>G
ENST00000698734.1:c.1767A>G ENSP00000513901.1:p.Leu589=
ENST00000698735.1:n.1882A>G
ENST00000698736.1:n.1882A>G
ENST00000698737.1:n.1882A>G
ENST00000698738.1:n.1882A>G
ENST00000698739.1:n.1882A>G
ENST00000372371.8:c.1767A>G MANE Select ENSP00000361446.3:p.Leu589=
ENST00000372371.7:c.1767A>G ENSP00000361446.3:p.Leu589=
ENST00000473588.2:c.569A>G
NM_007055.3:c.1767A>G NP_008986.2:p.Leu589=
NM_007055.4:c.1767A>G MANE Select NP_008986.2:p.Leu589=