ClinGen Allele Registry
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Canonical Allele Identifier:
CA211501556
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.93071756C>G
GRCh37
chr10:g.94831513C>G
Linked Data - Sequence & Population
gnomAD v2:
10:94831513 C / G
gnomAD v3:
10:93071756 C / G
gnomAD v4:
chr10-93071756-C-G
Joint Max Group AF
0.76854273 (EAS)
Genomes Max Group AF
0.76854273 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4411227
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.93071756C>G , CM000672.2:g.93071756C>G
GRCh38
NC_000010.10:g.94831513C>G , CM000672.1:g.94831513C>G
GRCh37
NC_000010.9:g.94821503C>G
NCBI36
NG_008067.1:g.3282C>G
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