ClinGen Allele Registry
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Canonical Allele Identifier:
CA14996194
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.23423078A>G
GRCh37
chr22:g.23765265A>G
Linked Data - Sequence & Population
gnomAD v2:
22:23765265 A / G
gnomAD v3:
22:23423078 A / G
gnomAD v4:
chr22-23423078-A-G
Joint Max Group AF
0.495365 (EAS)
Genomes Max Group AF
0.495365 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4822410
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.23423078A>G , CM000684.2:g.23423078A>G
GRCh38
NC_000022.10:g.23765265A>G , CM000684.1:g.23765265A>G
GRCh37
NC_000022.9:g.22095265A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'