Canonical Allele Identifier: CA2609821969

Gene: POLR3A

Linked Data

• gnomAD v4: 10-77999962-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77999962C>T , CM000672.2:g.77999962C>T	GRCh38
NC_000010.10:g.79759720C>T , CM000672.1:g.79759720C>T	GRCh37
NC_000010.9:g.79429726C>T	NCBI36
NG_029648.1:g.34579G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698727.1:n.1676+19G>A
ENST00000698728.1:n.2195+19G>A
ENST00000698729.1:n.3741+19G>A
ENST00000698730.1:n.3741+19G>A
ENST00000698731.1:c.2475+19G>A	ENSP00000513898.1:n.2475+19G>A
ENST00000698732.1:c.*1477+19G>A	ENSP00000513899.1:n.*1477+19G>A
ENST00000698733.1:c.*1803+19G>A	ENSP00000513900.1:n.*1803+19G>A
ENST00000698734.1:c.2616+19G>A	ENSP00000513901.1:n.2616+19G>A
ENST00000698735.1:n.2731+19G>A
ENST00000698736.1:n.2731+19G>A
ENST00000698737.1:n.2731+19G>A
ENST00000698738.1:n.2731+19G>A
ENST00000698739.1:n.2731+19G>A
ENST00000372371.8:c.2616+19G>A MANE Select	ENSP00000361446.3:n.2616+19G>A
ENST00000372371.7:c.2616+19G>A	ENSP00000361446.3:n.2616+19G>A
ENST00000472014.5:n.469+4754G>A
NM_007055.3:c.2616+19G>A	NP_008986.2:n.2616+19G>A
NM_007055.4:c.2616+19G>A MANE Select	NP_008986.2:n.2616+19G>A