Canonical Allele Identifier: CA5571041

Gene: POLR3A

Linked Data

• dbSNP Id: rs758663237
• ExAC: 10:79752990 G / A
• gnomAD v2: 10-79752990-G-A
• gnomAD v3: 10-77993232-G-A
• gnomAD v4: 10-77993232-G-A
• MyVariant Identifiers: chr10:g.79752990G>A (hg19) ; chr10:g.77993232G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77993232G>A , CM000672.2:g.77993232G>A	GRCh38
NC_000010.10:g.79752990G>A , CM000672.1:g.79752990G>A	GRCh37
NC_000010.9:g.79422996G>A	NCBI36
NG_029648.1:g.41309C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698724.1:n.20C>T
ENST00000698727.1:n.1812C>T
ENST00000698728.1:n.2331C>T
ENST00000698729.1:n.3877C>T
ENST00000698730.1:n.3877C>T
ENST00000698731.1:c.2611C>T	ENSP00000513898.1:p.Pro871Ser
ENST00000698732.1:c.*1613C>T	ENSP00000513899.1:n.*1613C>T
ENST00000698733.1:c.*1939C>T	ENSP00000513900.1:n.*1939C>T
ENST00000698734.1:c.*276C>T	ENSP00000513901.1:n.*276C>T
ENST00000698735.1:n.2867C>T
ENST00000698736.1:n.2867C>T
ENST00000698737.1:n.2867C>T
ENST00000698738.1:n.2867C>T
ENST00000698739.1:n.2867C>T
ENST00000372371.8:c.2752C>T MANE Select	ENSP00000361446.3:p.Pro918Ser
ENST00000372371.7:c.2752C>T	ENSP00000361446.3:p.Pro918Ser
ENST00000472014.5:n.605C>T
NM_007055.3:c.2752C>T	NP_008986.2:p.Pro918Ser
NM_007055.4:c.2752C>T MANE Select	NP_008986.2:p.Pro918Ser