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Canonical Allele Identifier:
CA258863806
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr14:g.35405503del
GRCh37
chr14:g.35874709del
Linked Data - Sequence & Population
gnomAD v2:
14:35874708 GA / G
gnomAD v3:
14:35405502 GA / G
gnomAD v4:
chr14-35405502-GA-G
Joint Max Group AF
0.16595947 (EAS)
Genomes Max Group AF
0.16595947 (EAS)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001518410
ClinVar Variation:
1168279
dbSNP:
17103265
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.35405505del , CM000676.2:g.35405505del
GRCh38
NC_000014.8:g.35874711del , CM000676.1:g.35874711del
GRCh37
NC_000014.7:g.34944462del
NCBI36
NG_007571.1:g.4236del , LRG_89:g.4236del
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