Canonical Allele Identifier: CA2722039574
Gene: POLR3A HGNC NCBI

Linked Data

dbSNP Id: rs1296578567

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77999866A>C , CM000672.2:g.77999866A>C GRCh38
NC_000010.10:g.79759624A>C , CM000672.1:g.79759624A>C GRCh37
NC_000010.9:g.79429630A>C NCBI36
NG_029648.1:g.34675T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698727.1:n.1676+115T>G
ENST00000698728.1:n.2195+115T>G
ENST00000698729.1:n.3741+115T>G
ENST00000698730.1:n.3741+115T>G
ENST00000698731.1:c.2475+115T>G ENSP00000513898.1:n.2475+115T>G
ENST00000698732.1:c.*1477+115T>G ENSP00000513899.1:n.*1477+115T>G
ENST00000698733.1:c.*1803+115T>G ENSP00000513900.1:n.*1803+115T>G
ENST00000698734.1:c.2616+115T>G ENSP00000513901.1:n.2616+115T>G
ENST00000698735.1:n.2731+115T>G
ENST00000698736.1:n.2731+115T>G
ENST00000698737.1:n.2731+115T>G
ENST00000698738.1:n.2731+115T>G
ENST00000698739.1:n.2731+115T>G
ENST00000372371.8:c.2616+115T>G MANE Select ENSP00000361446.3:n.2616+115T>G
ENST00000372371.7:c.2616+115T>G ENSP00000361446.3:n.2616+115T>G
ENST00000472014.5:n.469+4850T>G
NM_007055.3:c.2616+115T>G NP_008986.2:n.2616+115T>G
NM_007055.4:c.2616+115T>G MANE Select NP_008986.2:n.2616+115T>G