ClinGen Allele Registry
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Canonical Allele Identifier:
CA27682465
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100719321A>G
GRCh37
chr1:g.101184877A>G
Linked Data - Sequence & Population
gnomAD v2:
1:101184877 A / G
gnomAD v3:
1:100719321 A / G
gnomAD v4:
chr1-100719321-A-G
Joint Max Group AF
0.00806764 (AFR)
Genomes Max Group AF
0.00806764 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3783605
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100719321A>G , CM000663.2:g.100719321A>G
GRCh38
NC_000001.10:g.101184877A>G , CM000663.1:g.101184877A>G
GRCh37
NC_000001.9:g.100957465A>G
NCBI36
NG_023034.2:g.4581A>G
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