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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA688528013
Gene: PARP11
HGNC
NCBI
Linked Data
dbSNP Id:
rs1196805284
gnomAD v3:
12-3804201-A-T
gnomAD v4:
12-3804201-A-T
MyVariant Identifiers:
chr12:g.3913367A>T (hg19)
chr12:g.3804201A>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.3804201A>T , CM000674.2:g.3804201A>T
GRCh38
NC_000012.11:g.3913367A>T , CM000674.1:g.3913367A>T
GRCh37
NC_000012.10:g.3783628A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000416739.5:c.*196+2687T>A
ENSP00000392392.1:n.*196+2687T>A
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