ClinGen Allele Registry
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Canonical Allele Identifier:
CA13322333
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.67884201A>G
GRCh37
chr10:g.69643959A>G
Linked Data - Sequence & Population
gnomAD v2:
10:69643959 A / G
gnomAD v3:
10:67884201 A / G
gnomAD v4:
chr10-67884201-A-G
Joint Max Group AF
0.27413741 (EAS)
Genomes Max Group AF
0.27413741 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3740051
2131461872
2131461874
2131461880
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.67884201A>G , CM000672.2:g.67884201A>G
GRCh38
NC_000010.10:g.69643959A>G , CM000672.1:g.69643959A>G
GRCh37
NC_000010.9:g.69313965A>G
NCBI36
NG_050664.1:g.4540A>G
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