Canonical Allele Identifier: CA10575524
Gene:

Linked Data

ClinVar Variation Id: 14221
ClinVar RCV Id: RCV000015289 RCV001384494
dbSNP Id: rs878853178
gnomAD v2: 9-35658012-A-AACCACGTCCTCAGCTTC
gnomAD v3: 9-35658015-A-AACCACGTCCTCAGCTTC
gnomAD v4: 9-35658015-A-AACCACGTCCTCAGCTTC
MyVariant Identifiers: chr9:g.35658013_35658029dup17 (hg19) chr9:g.35658012_35658013insACCACGTCCTCAGCTTC (hg19) chr9:g.35658016_35658032dup17 (hg38) chr9:g.35658015_35658016insACCACGTCCTCAGCTTC (hg38)
PubMed: PMID:14608646
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658018_35658034dup , CM000671.2:g.35658018_35658034dup GRCh38
NC_000009.11:g.35658015_35658031dup , CM000671.1:g.35658015_35658031dup GRCh37
NC_000009.10:g.35648015_35648031dup NCBI36
NG_017041.1:g.4987_5003dup , LRG_163:g.4987_5003dup
NG_033120.1:g.4729_4745dup
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