Canonical Allele Identifier: CA2012874980
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs1947074727
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804159A>T , CM000674.2:g.3804159A>T GRCh38
NC_000012.11:g.3913325A>T , CM000674.1:g.3913325A>T GRCh37
NC_000012.10:g.3783586A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2729T>A ENSP00000392392.1:n.*196+2729T>A
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