ClinGen Allele Registry
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Canonical Allele Identifier:
CA13386388
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.69547646A>G
GRCh37
chr11:g.69362414A>G
Linked Data - Sequence & Population
gnomAD v2:
11:69362414 A / G
gnomAD v3:
11:69547646 A / G
gnomAD v4:
chr11-69547646-A-G
Joint Max Group AF
0.63745203 (NFE)
Genomes Max Group AF
0.63745203 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1485993
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.69547646A>G , CM000673.2:g.69547646A>G
GRCh38
NC_000011.9:g.69362414A>G , CM000673.1:g.69362414A>G
GRCh37
NC_000011.8:g.69071595A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'