Canonical Allele Identifier: CA470398320
Gene: POLR3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79769688A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78009930A>T , CM000672.2:g.78009930A>T GRCh38
NC_000010.10:g.79769688A>T , CM000672.1:g.79769688A>T GRCh37
NC_000010.9:g.79439694A>T NCBI36
NG_029648.1:g.24611T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698728.1:n.1283T>A
ENST00000698729.1:n.2829T>A
ENST00000698730.1:n.2829T>A
ENST00000698731.1:c.1563T>A ENSP00000513898.1:p.Ile521=
ENST00000698732.1:c.*565T>A ENSP00000513899.1:n.*565T>A
ENST00000698733.1:c.*891T>A ENSP00000513900.1:n.*891T>A
ENST00000698734.1:c.1704T>A ENSP00000513901.1:p.Ile568=
ENST00000698735.1:n.1819T>A
ENST00000698736.1:n.1819T>A
ENST00000698737.1:n.1819T>A
ENST00000698738.1:n.1819T>A
ENST00000698739.1:n.1819T>A
ENST00000372371.8:c.1704T>A MANE Select ENSP00000361446.3:p.Ile568=
ENST00000372371.7:c.1704T>A ENSP00000361446.3:p.Ile568=
ENST00000473588.2:c.506T>A
NM_007055.3:c.1704T>A NP_008986.2:p.Ile568=
NM_007055.4:c.1704T>A MANE Select NP_008986.2:p.Ile568=