Canonical Allele Identifier: CA232069559
Gene: PARP11 HGNC NCBI

Linked Data

dbSNP Id: rs537226119
gnomAD v2: 12-3913384-A-G
gnomAD v3: 12-3804218-A-G
gnomAD v4: 12-3804218-A-G
MyVariant Identifiers: chr12:g.3913384A>G (hg19) chr12:g.3804218A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3804218A>G , CM000674.2:g.3804218A>G GRCh38
NC_000012.11:g.3913384A>G , CM000674.1:g.3913384A>G GRCh37
NC_000012.10:g.3783645A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000416739.5:c.*196+2670T>C ENSP00000392392.1:n.*196+2670T>C
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