ClinGen Allele Registry
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Canonical Allele Identifier:
CA191309742
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.23345349A>G
GRCh37
chr9:g.23345347A>G
Linked Data - Sequence & Population
gnomAD v2:
9:23345347 A / G
gnomAD v3:
9:23345349 A / G
gnomAD v4:
chr9-23345349-A-G
Joint Max Group AF
0.43234188 (EAS)
Genomes Max Group AF
0.43234188 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11794152
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.23345349A>G , CM000671.2:g.23345349A>G
GRCh38
NC_000009.11:g.23345347A>G , CM000671.1:g.23345347A>G
GRCh37
NC_000009.10:g.23335347A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'