ClinGen Allele Registry
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Canonical Allele Identifier:
CA166418368
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.122990126A>C
GRCh37
chr7:g.122630180A>C
Linked Data - Sequence & Population
gnomAD v2:
7:122630180 A / C
gnomAD v3:
7:122990126 A / C
gnomAD v4:
chr7-122990126-A-C
Joint Max Group AF
0.86166766 (AFR)
Genomes Max Group AF
0.86166766 (AFR)
Linked Data - NCBI & NCI
dbSNP:
846672
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.122990126A>C , CM000669.2:g.122990126A>C
GRCh38
NC_000007.13:g.122630180A>C , CM000669.1:g.122630180A>C
GRCh37
NC_000007.12:g.122417416A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'