Canonical Allele Identifier: CA5571224

Gene: POLR3A

Linked Data

• dbSNP Id: rs200214545
• ExAC: 10:79764662 A / G
• gnomAD v2: 10-79764662-A-G
• gnomAD v3: 10-78004904-A-G
• gnomAD v4: 10-78004904-A-G
• MyVariant Identifiers: chr10:g.79764662A>G (hg19) ; chr10:g.78004904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78004904A>G , CM000672.2:g.78004904A>G	GRCh38
NC_000010.10:g.79764662A>G , CM000672.1:g.79764662A>G	GRCh37
NC_000010.9:g.79434668A>G	NCBI36
NG_029648.1:g.29637T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698727.1:n.1135-16T>C
ENST00000698728.1:n.1654-16T>C
ENST00000698729.1:n.3200-16T>C
ENST00000698730.1:n.3200-16T>C
ENST00000698731.1:c.1934-16T>C	ENSP00000513898.1:n.1934-16T>C
ENST00000698732.1:c.*936-16T>C	ENSP00000513899.1:n.*936-16T>C
ENST00000698733.1:c.*1262-16T>C	ENSP00000513900.1:n.*1262-16T>C
ENST00000698734.1:c.2075-16T>C	ENSP00000513901.1:n.2075-16T>C
ENST00000698735.1:n.2190-16T>C
ENST00000698736.1:n.2190-16T>C
ENST00000698737.1:n.2190-16T>C
ENST00000698738.1:n.2190-16T>C
ENST00000698739.1:n.2190-16T>C
ENST00000372371.8:c.2075-16T>C MANE Select	ENSP00000361446.3:n.2075-16T>C
ENST00000372371.7:c.2075-16T>C	ENSP00000361446.3:n.2075-16T>C
ENST00000472014.5:n.297-16T>C
ENST00000473588.2:c.738-16T>C
NM_007055.3:c.2075-16T>C	NP_008986.2:n.2075-16T>C
NM_007055.4:c.2075-16T>C MANE Select	NP_008986.2:n.2075-16T>C