ClinGen Allele Registry
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Canonical Allele Identifier:
CA16293887
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.20822683C>T
GRCh37
chr7:g.20862302C>T
Linked Data - Sequence & Population
gnomAD v2:
7:20862302 C / T
gnomAD v3:
7:20822683 C / T
gnomAD v4:
chr7-20822683-C-T
Joint Max Group AF
0.67212798 (AFR)
Genomes Max Group AF
0.67212798 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2709736
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.20822683C>T , CM000669.2:g.20822683C>T
GRCh38
NC_000007.13:g.20862302C>T , CM000669.1:g.20862302C>T
GRCh37
NC_000007.12:g.20828827C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'