Canonical Allele Identifier: CA2012875049
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs1591749014

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804317T>A , CM000674.2:g.3804317T>A GRCh38
NC_000012.11:g.3913483T>A , CM000674.1:g.3913483T>A GRCh37
NC_000012.10:g.3783744T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2571A>T ENSP00000392392.1:n.*196+2571A>T