Canonical Allele Identifier: CA944185373
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs1947075319
gnomAD v3: 12-3804238-G-A
gnomAD v4: 12-3804238-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804238G>A , CM000674.2:g.3804238G>A GRCh38
NC_000012.11:g.3913404G>A , CM000674.1:g.3913404G>A GRCh37
NC_000012.10:g.3783665G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2650C>T ENSP00000392392.1:n.*196+2650C>T
Search 100 bp 5'
Search 100 bp 3'