Canonical Allele Identifier: CA232069551

Gene: PARP11

Linked Data

• dbSNP Id: rs1030431161
• MyVariant Identifiers: chr12:g.3913320C>G (hg19) ; chr12:g.3804154C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3804154C>G , CM000674.2:g.3804154C>G	GRCh38
NC_000012.11:g.3913320C>G , CM000674.1:g.3913320C>G	GRCh37
NC_000012.10:g.3783581C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416739.5:c.*196+2734G>C	ENSP00000392392.1:n.*196+2734G>C