ClinGen Allele Registry
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Canonical Allele Identifier:
CA289355830
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.22590529A>G
GRCh37
chr17:g.22089856A>G
Linked Data - Sequence & Population
gnomAD v2:
17:22089856 A / G
gnomAD v3:
17:22590529 A / G
gnomAD v4:
chr17-22590529-A-G
Joint Max Group AF
0.62043286 (AFR)
Genomes Max Group AF
0.62043286 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8079482
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.22590529A>G , CM000679.2:g.22590529A>G
GRCh38
NC_000017.10:g.22089856A>G , CM000679.1:g.22089856A>G
GRCh37
NC_000017.9:g.22013983A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'