ClinGen Allele Registry
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Canonical Allele Identifier:
CA225332808
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.86072696C>A
GRCh37
chr11:g.85783738C>A
Linked Data - Sequence & Population
gnomAD v2:
11:85783738 C / A
gnomAD v3:
11:86072696 C / A
gnomAD v4:
chr11-86072696-C-A
Joint Max Group AF
0.32619945 (AFR)
Genomes Max Group AF
0.32619945 (AFR)
Linked Data - NCBI & NCI
dbSNP:
621942
2119644413
2119644417
2119644433
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.86072696C>A , CM000673.2:g.86072696C>A
GRCh38
NC_000011.9:g.85783738C>A , CM000673.1:g.85783738C>A
GRCh37
NC_000011.8:g.85461386C>A
NCBI36
NG_028942.1:g.2186G>T
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