Canonical Allele Identifier: CA2725572940
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs2137989374
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804266A>C , CM000674.2:g.3804266A>C GRCh38
NC_000012.11:g.3913432A>C , CM000674.1:g.3913432A>C GRCh37
NC_000012.10:g.3783693A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416739.5:c.*196+2622T>G ENSP00000392392.1:n.*196+2622T>G
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