ClinGen Allele Registry
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Canonical Allele Identifier:
CA15592686
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.27309661T>C
GRCh37
chr9:g.27309659T>C
Linked Data - Sequence & Population
gnomAD v2:
9:27309659 T / C
gnomAD v3:
9:27309661 T / C
gnomAD v4:
chr9-27309661-T-C
Joint Max Group AF
0.2920351 (AMR)
Genomes Max Group AF
0.2920351 (AMR)
Linked Data - NCBI & NCI
dbSNP:
10967875
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.27309661T>C , CM000671.2:g.27309661T>C
GRCh38
NC_000009.11:g.27309659T>C , CM000671.1:g.27309659T>C
GRCh37
NC_000009.10:g.27299659T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'