Canonical Allele Identifier: CA232069562
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs1034040735
gnomAD v3: 12-3804246-T-C
gnomAD v4: 12-3804246-T-C
MyVariant Identifiers: chr12:g.3913412T>C (hg19) chr12:g.3804246T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804246T>C , CM000674.2:g.3804246T>C GRCh38
NC_000012.11:g.3913412T>C , CM000674.1:g.3913412T>C GRCh37
NC_000012.10:g.3783673T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2642A>G ENSP00000392392.1:n.*196+2642A>G
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