ClinGen Allele Registry
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Canonical Allele Identifier:
CA198901290
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806803A>C
GRCh37
chr9:g.117569083A>C
Linked Data - Sequence & Population
gnomAD v2:
9:117569083 A / C
gnomAD v3:
9:114806803 A / C
gnomAD v4:
chr9-114806803-A-C
Joint Max Group AF
0.0044723 (SAS)
Genomes Max Group AF
0.0044723 (SAS)
Linked Data - NCBI & NCI
dbSNP:
530090698
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806803A>C , CM000671.2:g.114806803A>C
GRCh38
NC_000009.11:g.117569083A>C , CM000671.1:g.117569083A>C
GRCh37
NC_000009.10:g.116608904A>C
NCBI36
NG_011488.2:g.4326T>G
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