ClinGen Allele Registry
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Canonical Allele Identifier:
CA192745748
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.35658022T>C
GRCh37
chr9:g.35658019T>C
Linked Data - Sequence & Population
gnomAD v2:
9:35658019 T / C
gnomAD v3:
9:35658022 T / C
gnomAD v4:
chr9-35658022-T-C
Joint Max Group AF
0.00004312 (NFE)
Genomes Max Group AF
0.00001973 (NFE)
Exomes Max Group AF
0.00004233 (NFE)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000610071
RCV000672983
RCV001239736
ClinVar Variation:
516512
dbSNP:
555890962
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.35658022T>C , CM000671.2:g.35658022T>C
GRCh38
NC_000009.11:g.35658019T>C , CM000671.1:g.35658019T>C
GRCh37
NC_000009.10:g.35648019T>C
NCBI36
NG_017041.1:g.4997A>G , LRG_163:g.4997A>G
NG_033120.1:g.4733T>C
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