Canonical Allele Identifier: CA2581065527
Gene: PARP11 HGNC NCBI
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2627G>T ENSP00000392392.1:n.*196+2627G>T
Search 100 bp 5'
Search 100 bp 3'