ClinGen Allele Registry
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Canonical Allele Identifier:
CA11505763
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.86867732A>G
GRCh37
chr3:g.86916882A>G
Linked Data - Sequence & Population
gnomAD v2:
3:86916882 A / G
gnomAD v3:
3:86867732 A / G
gnomAD v4:
chr3-86867732-A-G
Joint Max Group AF
0.60789259 (NFE)
Genomes Max Group AF
0.60789259 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7642134
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.86867732A>G , CM000665.2:g.86867732A>G
GRCh38
NC_000003.11:g.86916882A>G , CM000665.1:g.86916882A>G
GRCh37
NC_000003.10:g.86999572A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'