ClinGen Allele Registry
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Canonical Allele Identifier:
CA279705729
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.27399508A>G
GRCh37
chr16:g.27410829A>G
Linked Data - Sequence & Population
gnomAD v2:
16:27410829 A / G
gnomAD v3:
16:27399508 A / G
gnomAD v4:
chr16-27399508-A-G
Joint Max Group AF
0.85854625 (NFE)
Genomes Max Group AF
0.85854625 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2107357
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.27399508A>G , CM000678.2:g.27399508A>G
GRCh38
NC_000016.9:g.27410829A>G , CM000678.1:g.27410829A>G
GRCh37
NC_000016.8:g.27318330A>G
NCBI36
NG_012222.1:g.2107A>G
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