Canonical Allele Identifier: CA16434713
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs2058350
gnomAD v2: 12-3913427-C-T
gnomAD v3: 12-3804261-C-T
gnomAD v4: 12-3804261-C-T
MyVariant Identifiers: chr12:g.3913427C>T (hg19) chr12:g.3804261C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

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

Transcript Alleles

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