ClinGen Allele Registry
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Canonical Allele Identifier:
CA13046675
Gene:
Linked Data - Expert Curation
COSMIC:
COSN14763745 (not active)
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22134173C>T
GRCh37
chr9:g.22134172C>T
Linked Data - Sequence & Population
gnomAD v2:
9:22134172 C / T
gnomAD v3:
9:22134173 C / T
gnomAD v4:
chr9-22134173-C-T
Joint Max Group AF
0.60367489 (EAS)
Genomes Max Group AF
0.60367489 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10757283
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22134173C>T , CM000671.2:g.22134173C>T
GRCh38
NC_000009.11:g.22134172C>T , CM000671.1:g.22134172C>T
GRCh37
NC_000009.10:g.22124172C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'