ClinGen Allele Registry
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Canonical Allele Identifier:
CA11518818
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186841685C>G
GRCh37
chr3:g.186559474C>G
Linked Data - Sequence & Population
gnomAD v2:
3:186559474 C / G
gnomAD v3:
3:186841685 C / G
gnomAD v4:
chr3-186841685-C-G
Joint Max Group AF
0.25714 (SAS)
Genomes Max Group AF
0.25714 (SAS)
Linked Data - NCBI & NCI
dbSNP:
266729
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186841685C>G , CM000665.2:g.186841685C>G
GRCh38
NC_000003.11:g.186559474C>G , CM000665.1:g.186559474C>G
GRCh37
NC_000003.10:g.188042168C>G
NCBI36
NG_021140.1:g.4012C>G
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