Canonical Allele Identifier: CA2012875046
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs191491762

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804315C>A , CM000674.2:g.3804315C>A GRCh38
NC_000012.11:g.3913481C>A , CM000674.1:g.3913481C>A GRCh37
NC_000012.10:g.3783742C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2573G>T ENSP00000392392.1:n.*196+2573G>T