Canonical Allele Identifier: CA602942798

Gene: PARP11

Linked Data

• dbSNP Id: rs1246603730
• gnomAD v2: 12-3913469-G-A
• gnomAD v3: 12-3804303-G-A
• gnomAD v4: 12-3804303-G-A
• MyVariant Identifiers: chr12:g.3913469G>A (hg19) ; chr12:g.3804303G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3804303G>A , CM000674.2:g.3804303G>A	GRCh38
NC_000012.11:g.3913469G>A , CM000674.1:g.3913469G>A	GRCh37
NC_000012.10:g.3783730G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416739.5:c.*196+2585C>T	ENSP00000392392.1:n.*196+2585C>T