Canonical Allele Identifier: CA594424518

Gene: POLR3A

Linked Data

• dbSNP Id: rs1475103830
• gnomAD v2: 10-79735579-A-T
• gnomAD v3: 10-77975821-A-T
• gnomAD v4: 10-77975821-A-T
• MyVariant Identifiers: chr10:g.79735579A>T (hg19) ; chr10:g.77975821A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77975821A>T , CM000672.2:g.77975821A>T	GRCh38
NC_000010.10:g.79735579A>T , CM000672.1:g.79735579A>T	GRCh37
NC_000010.9:g.79405585A>T	NCBI36
NG_029648.1:g.58720T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.1941+4320T>A
ENST00000698725.1:n.3500T>A
ENST00000698726.1:n.5060T>A
ENST00000698727.1:n.4793T>A
ENST00000698728.1:n.5409T>A
ENST00000698729.1:n.6857T>A
ENST00000698730.1:n.6955T>A
ENST00000698731.1:c.*1657T>A	ENSP00000513898.1:n.*1657T>A
ENST00000698732.1:c.*4519T>A	ENSP00000513899.1:n.*4519T>A
ENST00000698733.1:c.*5017T>A	ENSP00000513900.1:n.*5017T>A
ENST00000698734.1:c.*4003T>A	ENSP00000513901.1:n.*4003T>A
ENST00000698735.1:n.6181T>A
ENST00000698736.1:n.6594T>A
ENST00000372371.8:c.*1657T>A MANE Select	ENSP00000361446.3:n.*1657T>A
ENST00000372371.7:c.*1657T>A	ENSP00000361446.3:n.*1657T>A
ENST00000616246.4:c.472+4320T>A	ENSP00000483738.1:n.472+4320T>A
NM_007055.3:c.*1657T>A	NP_008986.2:n.*1657T>A
NM_007055.4:c.*1657T>A MANE Select	NP_008986.2:n.*1657T>A