Canonical Allele Identifier: CA2012874986
Gene: PARP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804170A= , CM000674.2:g.3804170A= GRCh38
NC_000012.11:g.3913336A= , CM000674.1:g.3913336A= GRCh37
NC_000012.10:g.3783597A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2718T= ENSP00000392392.1:n.*196+2718T=