ClinGen Allele Registry
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Canonical Allele Identifier:
CA858981149
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114806806A>G
GRCh37
chr9:g.117569086A>G
Linked Data - Sequence & Population
gnomAD v3:
9:114806806 A / G
gnomAD v4:
chr9-114806806-A-G
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1294385091
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114806806A>G , CM000671.2:g.114806806A>G
GRCh38
NC_000009.11:g.117569086A>G , CM000671.1:g.117569086A>G
GRCh37
NC_000009.10:g.116608907A>G
NCBI36
NG_011488.2:g.4323T>C
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