ClinGen Allele Registry
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Canonical Allele Identifier:
CA13430457
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.117880025C>G
GRCh37
chr11:g.117750740C>G
Linked Data - Sequence & Population
gnomAD v2:
11:117750740 C / G
gnomAD v3:
11:117880025 C / G
gnomAD v4:
chr11-117880025-C-G
Joint Max Group AF
0.6484628 (EAS)
Genomes Max Group AF
0.6484628 (EAS)
Linked Data - NCBI & NCI
dbSNP:
497768
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.117880025C>G , CM000673.2:g.117880025C>G
GRCh38
NC_000011.9:g.117750740C>G , CM000673.1:g.117750740C>G
GRCh37
NC_000011.8:g.117255950C>G
NCBI36
NG_013071.1:g.2406G>C
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