ClinGen Allele Registry
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Canonical Allele Identifier:
CA325121554
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.46143764G>A
Linked Data - Sequence & Population
gnomAD v3:
22:46143764 G / A
gnomAD v4:
chr22-46143764-G-A
Joint Max Group AF
0.61111879 (AFR)
Genomes Max Group AF
0.61111879 (AFR)
Linked Data - NCBI & NCI
dbSNP:
135561
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.46143764G>A , CM000684.2:g.46143764G>A
GRCh38
Search 100 bp 5'
Search 100 bp 3'