Canonical Allele Identifier: CA2794351645
Gene: PARP11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804272C>G , CM000674.2:g.3804272C>G GRCh38
NC_000012.11:g.3913438C>G , CM000674.1:g.3913438C>G GRCh37
NC_000012.10:g.3783699C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2616G>C ENSP00000392392.1:n.*196+2616G>C
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