Canonical Allele Identifier: CA377326231

Gene: POLR3A

Linked Data

• dbSNP Id: rs758997758
• MyVariant Identifiers: chr10:g.79740030C>A (hg19) ; chr10:g.77980272C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77980272C>A , CM000672.2:g.77980272C>A	GRCh38
NC_000010.10:g.79740030C>A , CM000672.1:g.79740030C>A	GRCh37
NC_000010.9:g.79410036C>A	NCBI36
NG_029648.1:g.54269G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698724.1:n.1810G>T
ENST00000698725.1:n.1563G>T
ENST00000698726.1:n.3123G>T
ENST00000698727.1:n.2856G>T
ENST00000698728.1:n.3472G>T
ENST00000698729.1:n.4920G>T
ENST00000698730.1:n.5018G>T
ENST00000698731.1:c.3752G>T	ENSP00000513898.1:p.Gly1251Val
ENST00000698732.1:c.*2582G>T	ENSP00000513899.1:n.*2582G>T
ENST00000698733.1:c.*3080G>T	ENSP00000513900.1:n.*3080G>T
ENST00000698734.1:c.*2066G>T	ENSP00000513901.1:n.*2066G>T
ENST00000698735.1:n.4244G>T
ENST00000698736.1:n.4657G>T
ENST00000698737.1:n.4008G>T
ENST00000372371.8:c.3893G>T MANE Select	ENSP00000361446.3:p.Gly1298Val
ENST00000372371.7:c.3893G>T	ENSP00000361446.3:p.Gly1298Val
ENST00000616246.4:c.341G>T	ENSP00000483738.1:p.Gly114Val
NM_007055.3:c.3893G>T	NP_008986.2:p.Gly1298Val
NM_007055.4:c.3893G>T MANE Select	NP_008986.2:p.Gly1298Val