ClinGen Allele Registry
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Canonical Allele Identifier:
CA15993786
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.21624807T>C
GRCh37
chr22:g.21979096T>C
Linked Data - Sequence & Population
gnomAD v2:
22:21979096 T / C
gnomAD v3:
22:21624807 T / C
gnomAD v4:
chr22-21624807-T-C
Joint Max Group AF
0.49135425 (EAS)
Genomes Max Group AF
0.49135425 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11089637
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.21624807T>C , CM000684.2:g.21624807T>C
GRCh38
NC_000022.10:g.21979096T>C , CM000684.1:g.21979096T>C
GRCh37
NC_000022.9:g.20309096T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'