ClinGen Allele Registry
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Canonical Allele Identifier:
CA12697081
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.21984422T>C
GRCh37
chr7:g.22024040T>C
Linked Data - Sequence & Population
gnomAD v2:
7:22024040 T / C
gnomAD v3:
7:21984422 T / C
gnomAD v4:
chr7-21984422-T-C
Joint Max Group AF
0.46381974 (SAS)
Genomes Max Group AF
0.46381974 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1175000
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.21984422T>C , CM000669.2:g.21984422T>C
GRCh38
NC_000007.13:g.22024040T>C , CM000669.1:g.22024040T>C
GRCh37
NC_000007.12:g.21990565T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'