ClinGen Allele Registry
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Canonical Allele Identifier:
CA27681607
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718321C>G
GRCh37
chr1:g.101183877C>G
Linked Data - Sequence & Population
gnomAD v2:
1:101183877 C / G
gnomAD v3:
1:100718321 C / G
gnomAD v4:
chr1-100718321-C-G
Joint Max Group AF
0.00007899 (AFR)
Genomes Max Group AF
0.00007899 (AFR)
Linked Data - NCBI & NCI
dbSNP:
904339090
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718321C>G , CM000663.2:g.100718321C>G
GRCh38
NC_000001.10:g.101183877C>G , CM000663.1:g.101183877C>G
GRCh37
NC_000001.9:g.100956465C>G
NCBI36
NG_023034.2:g.3581C>G
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