Canonical Allele Identifier: CA232069560

Gene: PARP11

Linked Data

• dbSNP Id: rs372335898
• MyVariant Identifiers: chr12:g.3913388T>C (hg19) ; chr12:g.3804222T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3804222T>C , CM000674.2:g.3804222T>C	GRCh38
NC_000012.11:g.3913388T>C , CM000674.1:g.3913388T>C	GRCh37
NC_000012.10:g.3783649T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416739.5:c.*196+2666A>G	ENSP00000392392.1:n.*196+2666A>G