Canonical Allele Identifier: CA2012875038
Gene: PARP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804293T= , CM000674.2:g.3804293T= GRCh38
NC_000012.11:g.3913459T= , CM000674.1:g.3913459T= GRCh37
NC_000012.10:g.3783720T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2595A= ENSP00000392392.1:n.*196+2595A=