ClinGen Allele Registry
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Canonical Allele Identifier:
CA15287842
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169759718A>G
GRCh37
chr3:g.169477506A>G
Linked Data - Sequence & Population
gnomAD v2:
3:169477506 A / G
gnomAD v3:
3:169759718 A / G
gnomAD v4:
chr3-169759718-A-G
Joint Max Group AF
0.55565261 (EAS)
Genomes Max Group AF
0.55565261 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12638862
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169759718A>G , CM000665.2:g.169759718A>G
GRCh38
NC_000003.11:g.169477506A>G , CM000665.1:g.169477506A>G
GRCh37
NC_000003.10:g.170960200A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'