Canonical Allele Identifier: CA2722109238
Gene: POLR3A HGNC NCBI

Linked Data

dbSNP Id: rs2131925752

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77980404A>G , CM000672.2:g.77980404A>G GRCh38
NC_000010.10:g.79740162A>G , CM000672.1:g.79740162A>G GRCh37
NC_000010.9:g.79410168A>G NCBI36
NG_029648.1:g.54137T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698724.1:n.1809-131T>C
ENST00000698725.1:n.1431T>C
ENST00000698726.1:n.3122-131T>C
ENST00000698727.1:n.2855-131T>C
ENST00000698728.1:n.3471-131T>C
ENST00000698729.1:n.4919-131T>C
ENST00000698730.1:n.5017-131T>C
ENST00000698731.1:c.3751-131T>C ENSP00000513898.1:n.3751-131T>C
ENST00000698732.1:c.*2581-131T>C ENSP00000513899.1:n.*2581-131T>C
ENST00000698733.1:c.*3079-131T>C ENSP00000513900.1:n.*3079-131T>C
ENST00000698734.1:c.*2065-131T>C ENSP00000513901.1:n.*2065-131T>C
ENST00000698735.1:n.4243-131T>C
ENST00000698736.1:n.4656-131T>C
ENST00000698737.1:n.4007-131T>C
ENST00000372371.8:c.3892-131T>C MANE Select ENSP00000361446.3:n.3892-131T>C
ENST00000372371.7:c.3892-131T>C ENSP00000361446.3:n.3892-131T>C
ENST00000616246.4:c.340-131T>C ENSP00000483738.1:n.340-131T>C
NM_007055.3:c.3892-131T>C NP_008986.2:n.3892-131T>C
NM_007055.4:c.3892-131T>C MANE Select NP_008986.2:n.3892-131T>C