ClinGen Allele Registry
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Canonical Allele Identifier:
CA11180903
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.22901686C>A
GRCh37
chr2:g.23124558C>A
Linked Data - Sequence & Population
gnomAD v2:
2:23124558 C / A
gnomAD v3:
2:22901686 C / A
gnomAD v4:
chr2-22901686-C-A
Joint Max Group AF
0.9768648 (EAS)
Genomes Max Group AF
0.9768648 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10189050
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.22901686C>A , CM000664.2:g.22901686C>A
GRCh38
NC_000002.11:g.23124558C>A , CM000664.1:g.23124558C>A
GRCh37
NC_000002.10:g.22978063C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'