ClinGen Allele Registry
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Canonical Allele Identifier:
CA13566766
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.67582428A>G
GRCh37
chr11:g.67349899A>G
Linked Data - Sequence & Population
gnomAD v2:
11:67349899 A / G
gnomAD v3:
11:67582428 A / G
gnomAD v4:
chr11-67582428-A-G
Joint Max Group AF
0.4219434 (NFE)
Genomes Max Group AF
0.4219434 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6591256
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.67582428A>G , CM000673.2:g.67582428A>G
GRCh38
NC_000011.9:g.67349899A>G , CM000673.1:g.67349899A>G
GRCh37
NC_000011.8:g.67106475A>G
NCBI36
NG_012075.1:g.3834A>G , LRG_723:g.3834A>G
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