Canonical Allele Identifier: CA1921497601
Gene: POLR3A HGNC NCBI

Linked Data

dbSNP Id: rs913651416

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980385T>C , CM000672.2:g.77980385T>C GRCh38
NC_000010.10:g.79740143T>C , CM000672.1:g.79740143T>C GRCh37
NC_000010.9:g.79410149T>C NCBI36
NG_029648.1:g.54156A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1809-112A>G
ENST00000698725.1:n.1450A>G
ENST00000698726.1:n.3122-112A>G
ENST00000698727.1:n.2855-112A>G
ENST00000698728.1:n.3471-112A>G
ENST00000698729.1:n.4919-112A>G
ENST00000698730.1:n.5017-112A>G
ENST00000698731.1:c.3751-112A>G ENSP00000513898.1:n.3751-112A>G
ENST00000698732.1:c.*2581-112A>G ENSP00000513899.1:n.*2581-112A>G
ENST00000698733.1:c.*3079-112A>G ENSP00000513900.1:n.*3079-112A>G
ENST00000698734.1:c.*2065-112A>G ENSP00000513901.1:n.*2065-112A>G
ENST00000698735.1:n.4243-112A>G
ENST00000698736.1:n.4656-112A>G
ENST00000698737.1:n.4007-112A>G
ENST00000372371.8:c.3892-112A>G MANE Select ENSP00000361446.3:n.3892-112A>G
ENST00000372371.7:c.3892-112A>G ENSP00000361446.3:n.3892-112A>G
ENST00000616246.4:c.340-112A>G ENSP00000483738.1:n.340-112A>G
NM_007055.3:c.3892-112A>G NP_008986.2:n.3892-112A>G
NM_007055.4:c.3892-112A>G MANE Select NP_008986.2:n.3892-112A>G