ClinGen Allele Registry
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Canonical Allele Identifier:
CA262598311
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.73136374del
GRCh37
chr14:g.73603082del
Linked Data - Sequence & Population
gnomAD v2:
14:73603081 GC / G
gnomAD v3:
14:73136373 GC / G
gnomAD v4:
chr14-73136373-GC-G
Joint Max Group AF
0.07395511 (AFR)
Genomes Max Group AF
0.07395865 (AFR)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001518793
ClinVar Variation:
1168490
dbSNP:
148370307
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.73136378del , CM000676.2:g.73136378del
GRCh38
NC_000014.8:g.73603086del , CM000676.1:g.73603086del
GRCh37
NC_000014.7:g.72672839del
NCBI36
NG_007386.2:g.4908del
Search 100 bp 5'
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