ClinGen Allele Registry
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Canonical Allele Identifier:
CA87625118
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765305C>T
GRCh37
chr3:g.169483093C>T
Linked Data - Sequence & Population
gnomAD v2:
3:169483093 C / T
gnomAD v3:
3:169765305 C / T
gnomAD v4:
chr3-169765305-C-T
Joint Max Group AF
0.01833339 (AFR)
Genomes Max Group AF
0.01823128 (AFR)
Exomes Max Group AF
0.0171906 (AFR)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001545411
RCV001821874
RCV003940990
ClinVar Variation:
1186345
dbSNP:
116780570
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765305C>T , CM000665.2:g.169765305C>T
GRCh38
NC_000003.11:g.169483093C>T , CM000665.1:g.169483093C>T
GRCh37
NC_000003.10:g.170965787C>T
NCBI36
NG_016363.1:g.4756G>A , LRG_347:g.4756G>A
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