ClinGen Allele Registry
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Canonical Allele Identifier:
CA10765588
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.22159378T>G
GRCh37
chr1:g.22485871T>G
Linked Data - Sequence & Population
gnomAD v2:
1:22485871 T / G
gnomAD v3:
1:22159378 T / G
gnomAD v4:
chr1-22159378-T-G
Joint Max Group AF
0.49097475 (EAS)
Genomes Max Group AF
0.49097475 (EAS)
Linked Data - NCBI & NCI
dbSNP:
16826658
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.22159378T>G , CM000663.2:g.22159378T>G
GRCh38
NC_000001.10:g.22485871T>G , CM000663.1:g.22485871T>G
GRCh37
NC_000001.9:g.22358458T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'