Canonical Allele Identifier: CA232069565

Gene: PARP11

Linked Data

• dbSNP Id: rs528010256
• gnomAD v2: 12-3913442-A-G
• gnomAD v3: 12-3804276-A-G
• gnomAD v4: 12-3804276-A-G
• MyVariant Identifiers: chr12:g.3913442A>G (hg19) ; chr12:g.3804276A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3804276A>G , CM000674.2:g.3804276A>G	GRCh38
NC_000012.11:g.3913442A>G , CM000674.1:g.3913442A>G	GRCh37
NC_000012.10:g.3783703A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416739.5:c.*196+2612T>C	ENSP00000392392.1:n.*196+2612T>C