ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA79056411
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.87418182C>T
GRCh37
chr3:g.87467332C>T
Linked Data - Sequence & Population
gnomAD v2:
3:87467332 C / T
gnomAD v3:
3:87418182 C / T
gnomAD v4:
chr3-87418182-C-T
Joint Max Group AF
0.91084882 (EAS)
Genomes Max Group AF
0.91084882 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2055109
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.87418182C>T , CM000665.2:g.87418182C>T
GRCh38
NC_000003.11:g.87467332C>T , CM000665.1:g.87467332C>T
GRCh37
NC_000003.10:g.87550022C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'