ClinGen Allele Registry
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Canonical Allele Identifier:
CA15595387
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.117702866T>C
GRCh37
chr9:g.120465144T>C
Linked Data - Sequence & Population
gnomAD v2:
9:120465144 T / C
gnomAD v3:
9:117702866 T / C
gnomAD v4:
chr9-117702866-T-C
Joint Max Group AF
0.2339278 (EAS)
Genomes Max Group AF
0.2339278 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10759932
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.117702866T>C , CM000671.2:g.117702866T>C
GRCh38
NC_000009.11:g.120465144T>C , CM000671.1:g.120465144T>C
GRCh37
NC_000009.10:g.119504965T>C
NCBI36
NG_011475.1:g.3685T>C
NG_011475.2:g.3464T>C
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