ClinGen Allele Registry
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Canonical Allele Identifier:
CA674740960
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.2287532A>C
GRCh37
chr11:g.2308762A>C
Linked Data - Sequence & Population
gnomAD v3:
11:2287532 A / C
gnomAD v4:
chr11-2287532-A-C
Joint Max Group AF
0.00001175 (NFE)
Genomes Max Group AF
0.00001175 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2521263
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2287532A>C , CM000673.2:g.2287532A>C
GRCh38
NC_000011.9:g.2308762A>C , CM000673.1:g.2308762A>C
GRCh37
NC_000011.8:g.2265338A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'