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Canonical Allele Identifier:
CA47858130
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.53275637A>G
GRCh37
chr2:g.53502775A>G
Linked Data - Sequence & Population
gnomAD v2:
2:53502775 A / G
gnomAD v3:
2:53275637 A / G
gnomAD v4:
chr2-53275637-A-G
Joint Max Group AF
0.52665207 (AFR)
Genomes Max Group AF
0.52665207 (AFR)
Linked Data - NCBI & NCI
dbSNP:
996712
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.53275637A>G , CM000664.2:g.53275637A>G
GRCh38
NC_000002.11:g.53502775A>G , CM000664.1:g.53502775A>G
GRCh37
NC_000002.10:g.53356279A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'