ClinGen Allele Registry
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Canonical Allele Identifier:
CA590283359
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806917C>T
GRCh37
chr9:g.117569197C>T
Linked Data - Sequence & Population
gnomAD v2:
9:117569197 C / T
gnomAD v3:
9:114806917 C / T
gnomAD v4:
chr9-114806917-C-T
Joint Max Group AF
0.00003249 (AFR)
Genomes Max Group AF
0.00003249 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1278528082
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806917C>T , CM000671.2:g.114806917C>T
GRCh38
NC_000009.11:g.117569197C>T , CM000671.1:g.117569197C>T
GRCh37
NC_000009.10:g.116609018C>T
NCBI36
NG_011488.2:g.4212G>A
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