ClinGen Allele Registry
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Canonical Allele Identifier:
CA15682663
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.57595235A>G
GRCh37
chr11:g.57362708A>G
Linked Data - Sequence & Population
gnomAD v2:
11:57362708 A / G
gnomAD v3:
11:57595235 A / G
gnomAD v4:
chr11-57595235-A-G
Joint Max Group AF
0.82836297 (EAS)
Genomes Max Group AF
0.82836297 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2511990
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.57595235A>G , CM000673.2:g.57595235A>G
GRCh38
NC_000011.9:g.57362708A>G , CM000673.1:g.57362708A>G
GRCh37
NC_000011.8:g.57119284A>G
NCBI36
NG_009625.1:g.2682A>G , LRG_105:g.2682A>G
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