ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA188348418
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.4482706T>A
GRCh37
chr9:g.4482706T>A
Linked Data - Sequence & Population
gnomAD v2:
9:4482706 T / A
gnomAD v3:
9:4482706 T / A
gnomAD v4:
chr9-4482706-T-A
Joint Max Group AF
0.00026013 (AFR)
Genomes Max Group AF
0.00026013 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10491734
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.4482706T>A , CM000671.2:g.4482706T>A
GRCh38
NC_000009.11:g.4482706T>A , CM000671.1:g.4482706T>A
GRCh37
NC_000009.10:g.4472706T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'