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Canonical Allele Identifier:
CA161451958
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.80227095T>C
GRCh37
chr7:g.79856411T>C
Linked Data - Sequence & Population
gnomAD v2:
7:79856411 T / C
gnomAD v3:
7:80227095 T / C
gnomAD v4:
chr7-80227095-T-C
Joint Max Group AF
0.78379498 (EAS)
Genomes Max Group AF
0.78379498 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2886609
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.80227095T>C , CM000669.2:g.80227095T>C
GRCh38
NC_000007.13:g.79856411T>C , CM000669.1:g.79856411T>C
GRCh37
NC_000007.12:g.79694347T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'