ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14928522
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.43110259T>A
GRCh37
chr22:g.43506265T>A
Linked Data - Sequence & Population
gnomAD v2:
22:43506265 T / A
gnomAD v3:
22:43110259 T / A
gnomAD v4:
chr22-43110259-T-A
Joint Max Group AF
0.86431187 (AFR)
Genomes Max Group AF
0.86431187 (AFR)
Linked Data - NCBI & NCI
dbSNP:
926328
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.43110259T>A , CM000684.2:g.43110259T>A
GRCh38
NC_000022.10:g.43506265T>A , CM000684.1:g.43506265T>A
GRCh37
NC_000022.9:g.41836209T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'