ClinGen Allele Registry
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Canonical Allele Identifier:
CA587100590
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22134008del
GRCh37
chr9:g.22134007del
Linked Data - Sequence & Population
gnomAD v2:
9:22134006 CA / C
gnomAD v3:
9:22134007 CA / C
gnomAD v4:
chr9-22134007-CA-C
Linked Data - NCBI & NCI
dbSNP:
1235610832
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22134008del , CM000671.2:g.22134008del
GRCh38
NC_000009.11:g.22134007del , CM000671.1:g.22134007del
GRCh37
NC_000009.10:g.22124007del
NCBI36
Search 100 bp 5'
Search 100 bp 3'