ClinGen Allele Registry
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Canonical Allele Identifier:
CA13008941
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22124478A>G
GRCh37
chr9:g.22124477A>G
Linked Data - Sequence & Population
gnomAD v2:
9:22124477 A / G
gnomAD v3:
9:22124478 A / G
gnomAD v4:
chr9-22124478-A-G
Joint Max Group AF
0.50829906 (SAS)
Genomes Max Group AF
0.50829906 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10757278
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22124478A>G , CM000671.2:g.22124478A>G
GRCh38
NC_000009.11:g.22124477A>G , CM000671.1:g.22124477A>G
GRCh37
NC_000009.10:g.22114477A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'