ClinGen Allele Registry
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Canonical Allele Identifier:
CA12474594
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.86642700T>A
GRCh37
chr7:g.86272016T>A
Linked Data - Sequence & Population
gnomAD v2:
7:86272016 T / A
gnomAD v3:
7:86642700 T / A
gnomAD v4:
chr7-86642700-T-A
Joint Max Group AF
0.85786205 (EAS)
Genomes Max Group AF
0.85786205 (EAS)
Linked Data - NCBI & NCI
dbSNP:
274618
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.86642700T>A , CM000669.2:g.86642700T>A
GRCh38
NC_000007.13:g.86272016T>A , CM000669.1:g.86272016T>A
GRCh37
NC_000007.12:g.86109952T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'