ClinGen Allele Registry
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Canonical Allele Identifier:
CA12998288
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.114321523C>A
GRCh37
chr9:g.117083803C>A
Linked Data - Sequence & Population
gnomAD v2:
9:117083803 C / A
gnomAD v3:
9:114321523 C / A
gnomAD v4:
chr9-114321523-C-A
Joint Max Group AF
0.07310959 (NFE)
Genomes Max Group AF
0.07310959 (NFE)
Linked Data - NCBI & NCI
dbSNP:
150611042
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114321523C>A , CM000671.2:g.114321523C>A
GRCh38
NC_000009.11:g.117083803C>A , CM000671.1:g.117083803C>A
GRCh37
NC_000009.10:g.116123624C>A
NCBI36
NG_012108.1:g.3501C>A
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