ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA16004333
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.29451733C>A
GRCh37
chr22:g.29847722C>A
Linked Data - Sequence & Population
gnomAD v2:
22:29847722 C / A
gnomAD v3:
22:29451733 C / A
gnomAD v4:
chr22-29451733-C-A
Joint Max Group AF
0.23992946 (AFR)
Genomes Max Group AF
0.23992946 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13053817
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.29451733C>A , CM000684.2:g.29451733C>A
GRCh38
NC_000022.10:g.29847722C>A , CM000684.1:g.29847722C>A
GRCh37
NC_000022.9:g.28177722C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'