ClinGen Allele Registry
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Canonical Allele Identifier:
CA16373277
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.117700861A>G
GRCh37
chr9:g.120463139A>G
Linked Data - Sequence & Population
gnomAD v2:
9:120463139 A / G
gnomAD v3:
9:117700861 A / G
gnomAD v4:
chr9-117700861-A-G
Joint Max Group AF
0.27757007 (NFE)
Genomes Max Group AF
0.27757007 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2770150
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.117700861A>G , CM000671.2:g.117700861A>G
GRCh38
NC_000009.11:g.120463139A>G , CM000671.1:g.120463139A>G
GRCh37
NC_000009.10:g.119502960A>G
NCBI36
NG_011475.1:g.1680A>G
NG_011475.2:g.1459A>G
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