ClinGen Allele Registry
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Canonical Allele Identifier:
CA16429736
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113974819A>G
GRCh37
chr11:g.113845541A>G
Linked Data - Sequence & Population
gnomAD v2:
11:113845541 A / G
gnomAD v3:
11:113974819 A / G
gnomAD v4:
chr11-113974819-A-G
Joint Max Group AF
0.98460115 (EAS)
Genomes Max Group AF
0.97659596 (EAS)
Exomes Max Group AF
0.97989324 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1150226
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113974819A>G , CM000673.2:g.113974819A>G
GRCh38
NC_000011.9:g.113845541A>G , CM000673.1:g.113845541A>G
GRCh37
NC_000011.8:g.113350751A>G
NCBI36
NG_013058.1:g.4745A>G
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