Canonical Allele Identifier: CA2590713628
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs2137989301
gnomAD v3: 12-3804175-C-A
gnomAD v4: 12-3804175-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804175C>A , CM000674.2:g.3804175C>A GRCh38
NC_000012.11:g.3913341C>A , CM000674.1:g.3913341C>A GRCh37
NC_000012.10:g.3783602C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000416739.5:c.*196+2713G>T ENSP00000392392.1:n.*196+2713G>T
Search 100 bp 5'
Search 100 bp 3'