ClinGen Allele Registry
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Canonical Allele Identifier:
CA13532624
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.64778919C>T
GRCh37
chr11:g.64546391C>T
Linked Data - Sequence & Population
gnomAD v2:
11:64546391 C / T
gnomAD v3:
11:64778919 C / T
gnomAD v4:
chr11-64778919-C-T
Joint Max Group AF
0.89130305 (NFE)
Genomes Max Group AF
0.89200067 (NFE)
Exomes Max Group AF
0.8740474 (NFE)
Linked Data - NCBI & NCI
dbSNP:
606458
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.64778919C>T , CM000673.2:g.64778919C>T
GRCh38
NC_000011.9:g.64546391C>T , CM000673.1:g.64546391C>T
GRCh37
NC_000011.8:g.64302967C>T
NCBI36
NG_021399.1:g.4926G>A , LRG_617:g.4926G>A
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