Canonical Allele Identifier: CA470394821
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79752997T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77993239T>C , CM000672.2:g.77993239T>C GRCh38
NC_000010.10:g.79752997T>C , CM000672.1:g.79752997T>C GRCh37
NC_000010.9:g.79423003T>C NCBI36
NG_029648.1:g.41302A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698724.1:n.13A>G
ENST00000698727.1:n.1805A>G
ENST00000698728.1:n.2324A>G
ENST00000698729.1:n.3870A>G
ENST00000698730.1:n.3870A>G
ENST00000698731.1:c.2604A>G ENSP00000513898.1:p.Lys868=
ENST00000698732.1:c.*1606A>G ENSP00000513899.1:n.*1606A>G
ENST00000698733.1:c.*1932A>G ENSP00000513900.1:n.*1932A>G
ENST00000698734.1:c.*269A>G ENSP00000513901.1:n.*269A>G
ENST00000698735.1:n.2860A>G
ENST00000698736.1:n.2860A>G
ENST00000698737.1:n.2860A>G
ENST00000698738.1:n.2860A>G
ENST00000698739.1:n.2860A>G
ENST00000372371.8:c.2745A>G MANE Select ENSP00000361446.3:p.Lys915=
ENST00000372371.7:c.2745A>G ENSP00000361446.3:p.Lys915=
ENST00000472014.5:n.598A>G
NM_007055.3:c.2745A>G NP_008986.2:p.Lys915=
NM_007055.4:c.2745A>G MANE Select NP_008986.2:p.Lys915=