ClinGen Allele Registry
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Canonical Allele Identifier:
CA15716684
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.64589600T>C
GRCh37
chr11:g.64357072T>C
Linked Data - Sequence & Population
gnomAD v2:
11:64357072 T / C
gnomAD v3:
11:64589600 T / C
gnomAD v4:
chr11-64589600-T-C
Joint Max Group AF
0.75829774 (EAS)
Genomes Max Group AF
0.75829774 (EAS)
Linked Data - NCBI & NCI
dbSNP:
505802
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.64589600T>C , CM000673.2:g.64589600T>C
GRCh38
NC_000011.9:g.64357072T>C , CM000673.1:g.64357072T>C
GRCh37
NC_000011.8:g.64113648T>C
NCBI36
NG_008110.1:g.3791T>C
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