ClinGen Allele Registry
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Canonical Allele Identifier:
CA15694258
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.65889093C>T
GRCh37
chr11:g.65656564C>T
Linked Data - Sequence & Population
gnomAD v2:
11:65656564 C / T
gnomAD v3:
11:65889093 C / T
gnomAD v4:
chr11-65889093-C-T
Joint Max Group AF
0.31551694 (EAS)
Genomes Max Group AF
0.31551694 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2231884
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.65889093C>T , CM000673.2:g.65889093C>T
GRCh38
NC_000011.9:g.65656564C>T , CM000673.1:g.65656564C>T
GRCh37
NC_000011.8:g.65413140C>T
NCBI36
NG_047103.1:g.4447G>A
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