Canonical Allele Identifier: CA232069558
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs150680014
gnomAD v2: 12-3913361-G-T
gnomAD v3: 12-3804195-G-T
gnomAD v4: 12-3804195-G-T
MyVariant Identifiers: chr12:g.3913361G>T (hg19) chr12:g.3804195G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804195G>T , CM000674.2:g.3804195G>T GRCh38
NC_000012.11:g.3913361G>T , CM000674.1:g.3913361G>T GRCh37
NC_000012.10:g.3783622G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000416739.5:c.*196+2693C>A ENSP00000392392.1:n.*196+2693C>A
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