ClinGen Allele Registry
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Canonical Allele Identifier:
CA590283340
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806724A>G
GRCh37
chr9:g.117569004A>G
Linked Data - Sequence & Population
gnomAD v2:
9:117569004 A / G
gnomAD v3:
9:114806724 A / G
gnomAD v4:
chr9-114806724-A-G
Joint Max Group AF
0.00006285 (AFR)
Genomes Max Group AF
0.00006285 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1381203002
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806724A>G , CM000671.2:g.114806724A>G
GRCh38
NC_000009.11:g.117569004A>G , CM000671.1:g.117569004A>G
GRCh37
NC_000009.10:g.116608825A>G
NCBI36
NG_011488.2:g.4405T>C
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