Canonical Allele Identifier: CA2012874968
Gene: PARP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804139A= , CM000674.2:g.3804139A= GRCh38
NC_000012.11:g.3913305A= , CM000674.1:g.3913305A= GRCh37
NC_000012.10:g.3783566A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2749T= ENSP00000392392.1:n.*196+2749T=