Canonical Allele Identifier: CA654074256
Gene: PARP11 HGNC NCBI

Linked Data

COSMIC: COSN18909948
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804185G>A , CM000674.2:g.3804185G>A GRCh38
NC_000012.11:g.3913351G>A , CM000674.1:g.3913351G>A GRCh37
NC_000012.10:g.3783612G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2703C>T ENSP00000392392.1:n.*196+2703C>T
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