ClinGen Allele Registry
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Canonical Allele Identifier:
CA166312836
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.126129532A>T
GRCh37
chr7:g.125769586A>T
Linked Data - Sequence & Population
gnomAD v2:
7:125769586 A / T
gnomAD v3:
7:126129532 A / T
gnomAD v4:
chr7-126129532-A-T
Joint Max Group AF
0.00022304 (AFR)
Genomes Max Group AF
0.00022304 (AFR)
Linked Data - NCBI & NCI
dbSNP:
586586
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.126129532A>T , CM000669.2:g.126129532A>T
GRCh38
NC_000007.13:g.125769586A>T , CM000669.1:g.125769586A>T
GRCh37
NC_000007.12:g.125556822A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'