ClinGen Allele Registry
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Canonical Allele Identifier:
CA15276820
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.56701152C>A
GRCh37
chr3:g.56735180C>A
Linked Data - Sequence & Population
gnomAD v2:
3:56735180 C / A
gnomAD v3:
3:56701152 C / A
gnomAD v4:
chr3-56701152-C-A
Joint Max Group AF
0.84216126 (EAS)
Genomes Max Group AF
0.84216126 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6773931
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.56701152C>A , CM000665.2:g.56701152C>A
GRCh38
NC_000003.11:g.56735180C>A , CM000665.1:g.56735180C>A
GRCh37
NC_000003.10:g.56710220C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'