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Canonical Allele Identifier:
CA89682749
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.186867738C>A
GRCh37
chr3:g.186585527C>A
Linked Data - Sequence & Population
gnomAD v3:
3:186867738 C / A
gnomAD v4:
chr3-186867738-C-A
Joint Max Group AF
0.00012876 (AMR)
Genomes Max Group AF
0.00012876 (AMR)
Linked Data - NCBI & NCI
dbSNP:
17373414
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.186867738C>A , CM000665.2:g.186867738C>A
GRCh38
NC_000003.11:g.186585527C>A , CM000665.1:g.186585527C>A
GRCh37
NC_000003.10:g.188068221C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'