Canonical Allele Identifier: CA944185361
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs1947075023
gnomAD v3: 12-3804199-C-G
gnomAD v4: 12-3804199-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804199C>G , CM000674.2:g.3804199C>G GRCh38
NC_000012.11:g.3913365C>G , CM000674.1:g.3913365C>G GRCh37
NC_000012.10:g.3783626C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2689G>C ENSP00000392392.1:n.*196+2689G>C