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Canonical Allele Identifier:
CA27681618
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.100718331C>T
GRCh37
chr1:g.101183887C>T
Linked Data - Sequence & Population
gnomAD v2:
1:101183887 C / T
gnomAD v3:
1:100718331 C / T
gnomAD v4:
chr1-100718331-C-T
Joint Max Group AF
0.05023778 (AFR)
Genomes Max Group AF
0.05023778 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3783599
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.100718331C>T , CM000663.2:g.100718331C>T
GRCh38
NC_000001.10:g.101183887C>T , CM000663.1:g.101183887C>T
GRCh37
NC_000001.9:g.100956475C>T
NCBI36
NG_023034.2:g.3591C>T
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