Canonical Allele Identifier: CA688528086

Gene: PARP11

Linked Data

• dbSNP Id: rs1170913266
• gnomAD v3: 12-3804302-C-T
• gnomAD v4: 12-3804302-C-T
• MyVariant Identifiers: chr12:g.3913468C>T (hg19) ; chr12:g.3804302C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3804302C>T , CM000674.2:g.3804302C>T	GRCh38
NC_000012.11:g.3913468C>T , CM000674.1:g.3913468C>T	GRCh37
NC_000012.10:g.3783729C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416739.5:c.*196+2586G>A	ENSP00000392392.1:n.*196+2586G>A