ClinGen Allele Registry
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Canonical Allele Identifier:
CA15929369
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.23026633T>C
GRCh37
chr18:g.20606596T>C
Linked Data - Sequence & Population
gnomAD v2:
18:20606596 T / C
gnomAD v3:
18:23026633 T / C
gnomAD v4:
chr18-23026633-T-C
Joint Max Group AF
0.8100857 (MID)
Genomes Max Group AF
0.77246677 (NFE)
Exomes Max Group AF
0.7575014 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9304261
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.23026633T>C , CM000680.2:g.23026633T>C
GRCh38
NC_000018.9:g.20606596T>C , CM000680.1:g.20606596T>C
GRCh37
NC_000018.8:g.18860594T>C
NCBI36
NG_012121.1:g.98302T>C
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