ClinGen Allele Registry
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Canonical Allele Identifier:
CA15649965
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.67883859A>C
GRCh37
chr10:g.69643617A>C
Linked Data - Sequence & Population
gnomAD v2:
10:69643617 A / C
gnomAD v3:
10:67883859 A / C
gnomAD v4:
chr10-67883859-A-C
Joint Max Group AF
0.16000437 (SAS)
Genomes Max Group AF
0.16000437 (SAS)
Linked Data - NCBI & NCI
dbSNP:
35706870
2131461836
2131461839
2131461843
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.67883859A>C , CM000672.2:g.67883859A>C
GRCh38
NC_000010.10:g.69643617A>C , CM000672.1:g.69643617A>C
GRCh37
NC_000010.9:g.69313623A>C
NCBI36
NG_050664.1:g.4198A>C
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