Canonical Allele Identifier: CA688528043

Gene: PARP11

Linked Data

• dbSNP Id: rs1213976363
• MyVariant Identifiers: chr12:g.3913397C>A (hg19) ; chr12:g.3804231C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3804231C>A , CM000674.2:g.3804231C>A	GRCh38
NC_000012.11:g.3913397C>A , CM000674.1:g.3913397C>A	GRCh37
NC_000012.10:g.3783658C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416739.5:c.*196+2657G>T	ENSP00000392392.1:n.*196+2657G>T