ClinGen Allele Registry
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Canonical Allele Identifier:
CA212839790
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr10:g.99861014C>G
GRCh37
chr10:g.101620771C>G
Linked Data - Sequence & Population
gnomAD v2:
10:101620771 C / G
gnomAD v3:
10:99861014 C / G
gnomAD v4:
chr10-99861014-C-G
Joint Max Group AF
0.55474326 (EAS)
Genomes Max Group AF
0.55474326 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12762549
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99861014C>G , CM000672.2:g.99861014C>G
GRCh38
NC_000010.10:g.101620771C>G , CM000672.1:g.101620771C>G
GRCh37
NC_000010.9:g.101610761C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'