Canonical Allele Identifier: CA594710651

Gene: POLR3A

Linked Data

• dbSNP Id: rs1172276909
• gnomAD v2: 10-79769757-T-A
• gnomAD v4: 10-78009999-T-A
• MyVariant Identifiers: chr10:g.79769757T>A (hg19) ; chr10:g.78009999T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78009999T>A , CM000672.2:g.78009999T>A	GRCh38
NC_000010.10:g.79769757T>A , CM000672.1:g.79769757T>A	GRCh37
NC_000010.9:g.79439763T>A	NCBI36
NG_029648.1:g.24542A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698728.1:n.1222-8A>T
ENST00000698729.1:n.2768-8A>T
ENST00000698730.1:n.2768-8A>T
ENST00000698731.1:c.1502-8A>T	ENSP00000513898.1:n.1502-8A>T
ENST00000698732.1:c.*504-8A>T	ENSP00000513899.1:n.*504-8A>T
ENST00000698733.1:c.*830-8A>T	ENSP00000513900.1:n.*830-8A>T
ENST00000698734.1:c.1643-8A>T	ENSP00000513901.1:n.1643-8A>T
ENST00000698735.1:n.1758-8A>T
ENST00000698736.1:n.1758-8A>T
ENST00000698737.1:n.1758-8A>T
ENST00000698738.1:n.1758-8A>T
ENST00000698739.1:n.1758-8A>T
ENST00000372371.8:c.1643-8A>T MANE Select	ENSP00000361446.3:n.1643-8A>T
ENST00000372371.7:c.1643-8A>T	ENSP00000361446.3:n.1643-8A>T
ENST00000473588.2:c.445-8A>T
NM_007055.3:c.1643-8A>T	NP_008986.2:n.1643-8A>T
NM_007055.4:c.1643-8A>T MANE Select	NP_008986.2:n.1643-8A>T