ClinGen Allele Registry
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Canonical Allele Identifier:
CA587100599
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22134111A>G
GRCh37
chr9:g.22134110A>G
Linked Data - Sequence & Population
gnomAD v2:
9:22134110 A / G
gnomAD v3:
9:22134111 A / G
gnomAD v4:
chr9-22134111-A-G
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1346502360
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22134111A>G , CM000671.2:g.22134111A>G
GRCh38
NC_000009.11:g.22134110A>G , CM000671.1:g.22134110A>G
GRCh37
NC_000009.10:g.22124110A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'