ClinGen Allele Registry
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Canonical Allele Identifier:
CA161017799
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.77967495T>C
GRCh37
chr7:g.77596812T>C
Linked Data - Sequence & Population
gnomAD v2:
7:77596812 T / C
gnomAD v3:
7:77967495 T / C
gnomAD v4:
chr7-77967495-T-C
Joint Max Group AF
0.89750334 (NFE)
Genomes Max Group AF
0.89750334 (NFE)
Linked Data - NCBI & NCI
dbSNP:
848452
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.77967495T>C , CM000669.2:g.77967495T>C
GRCh38
NC_000007.13:g.77596812T>C , CM000669.1:g.77596812T>C
GRCh37
NC_000007.12:g.77434748T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'