ClinGen Allele Registry
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Canonical Allele Identifier:
CA197107308
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.99472041C>A
GRCh37
chr9:g.102234323C>A
Linked Data - Sequence & Population
gnomAD v2:
9:102234323 C / A
gnomAD v3:
9:99472041 C / A
gnomAD v4:
chr9-99472041-C-A
Joint Max Group AF
0.17297953 (AMR)
Genomes Max Group AF
0.17297953 (AMR)
Linked Data - NCBI & NCI
dbSNP:
649057
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.99472041C>A , CM000671.2:g.99472041C>A
GRCh38
NC_000009.11:g.102234323C>A , CM000671.1:g.102234323C>A
GRCh37
NC_000009.10:g.101274144C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'