ClinGen Allele Registry
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Canonical Allele Identifier:
CA200772667
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.133279294T>G
Linked Data - Sequence & Population
gnomAD v3:
9:133279294 T / G
gnomAD v4:
chr9-133279294-T-G
Joint Max Group AF
0.85600846 (AFR)
Genomes Max Group AF
0.85600846 (AFR)
Linked Data - NCBI & NCI
dbSNP:
495828
2129834604
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133279294T>G , CM000671.2:g.133279294T>G
GRCh38
NG_006669.2:g.921A>C
Search 100 bp 5'
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