Canonical Allele Identifier: CA2581065526
Gene: PARP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804261C>G , CM000674.2:g.3804261C>G GRCh38
NC_000012.11:g.3913427C>G , CM000674.1:g.3913427C>G GRCh37
NC_000012.10:g.3783688C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2627G>C ENSP00000392392.1:n.*196+2627G>C