ClinGen Allele Registry
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Canonical Allele Identifier:
CA161066815
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.80711306C>A
GRCh37
chr7:g.80340622C>A
Linked Data - Sequence & Population
gnomAD v2:
7:80340622 C / A
gnomAD v3:
7:80711306 C / A
gnomAD v4:
chr7-80711306-C-A
Joint Max Group AF
0.99299772 (NFE)
Genomes Max Group AF
0.99299772 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2366858
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.80711306C>A , CM000669.2:g.80711306C>A
GRCh38
NC_000007.13:g.80340622C>A , CM000669.1:g.80340622C>A
GRCh37
NC_000007.12:g.80178558C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'