ClinGen Allele Registry
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Canonical Allele Identifier:
CA11365083
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.66748526C>G
GRCh37
chr3:g.66798950C>G
Linked Data - Sequence & Population
gnomAD v2:
3:66798950 C / G
gnomAD v3:
3:66748526 C / G
gnomAD v4:
chr3-66748526-C-G
Joint Max Group AF
0.18356071 (NFE)
Genomes Max Group AF
0.18356071 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13069000
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.66748526C>G , CM000665.2:g.66748526C>G
GRCh38
NC_000003.11:g.66798950C>G , CM000665.1:g.66798950C>G
GRCh37
NC_000003.10:g.66881640C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'