ClinGen Allele Registry
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Canonical Allele Identifier:
CA13370227
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.2212344A>G
GRCh37
chr11:g.2233574A>G
Linked Data - Sequence & Population
gnomAD v2:
11:2233574 A / G
gnomAD v3:
11:2212344 A / G
gnomAD v4:
chr11-2212344-A-G
Joint Max Group AF
0.86994339 (EAS)
Genomes Max Group AF
0.86994339 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7127900
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2212344A>G , CM000673.2:g.2212344A>G
GRCh38
NC_000011.9:g.2233574A>G , CM000673.1:g.2233574A>G
GRCh37
NC_000011.8:g.2190150A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'