Canonical Allele Identifier: CA602942797
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs1331065272
gnomAD v2: 12-3913424-G-A
gnomAD v3: 12-3804258-G-A
gnomAD v4: 12-3804258-G-A
MyVariant Identifiers: chr12:g.3913424G>A (hg19) chr12:g.3804258G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804258G>A , CM000674.2:g.3804258G>A GRCh38
NC_000012.11:g.3913424G>A , CM000674.1:g.3913424G>A GRCh37
NC_000012.10:g.3783685G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2630C>T ENSP00000392392.1:n.*196+2630C>T
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