ClinGen Allele Registry
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Canonical Allele Identifier:
CA323862221
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.34493105T>G
GRCh37
chr22:g.34889097T>G
Linked Data - Sequence & Population
gnomAD v2:
22:34889097 T / G
gnomAD v3:
22:34493105 T / G
gnomAD v4:
chr22-34493105-T-G
Joint Max Group AF
0.16192609 (AFR)
Genomes Max Group AF
0.16192609 (AFR)
Linked Data - NCBI & NCI
dbSNP:
738968
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.34493105T>G , CM000684.2:g.34493105T>G
GRCh38
NC_000022.10:g.34889097T>G , CM000684.1:g.34889097T>G
GRCh37
NC_000022.9:g.33219097T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'