ClinGen Allele Registry
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Canonical Allele Identifier:
CA13015901
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.95666984C>G
GRCh37
chr9:g.98429266C>G
Linked Data - Sequence & Population
gnomAD v2:
9:98429266 C / G
gnomAD v3:
9:95666984 C / G
gnomAD v4:
chr9-95666984-C-G
Joint Max Group AF
0.20904237 (AFR)
Genomes Max Group AF
0.20904237 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11790994
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.95666984C>G , CM000671.2:g.95666984C>G
GRCh38
NC_000009.11:g.98429266C>G , CM000671.1:g.98429266C>G
GRCh37
NC_000009.10:g.97469087C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'