ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA191256832
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22133285G>A
GRCh37
chr9:g.22133284G>A
Linked Data - Sequence & Population
gnomAD v2:
9:22133284 G / A
gnomAD v3:
9:22133285 G / A
gnomAD v4:
chr9-22133285-G-A
Joint Max Group AF
0.39879601 (EAS)
Genomes Max Group AF
0.39879601 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10965250
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22133285G>A , CM000671.2:g.22133285G>A
GRCh38
NC_000009.11:g.22133284G>A , CM000671.1:g.22133284G>A
GRCh37
NC_000009.10:g.22123284G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'