Canonical Allele Identifier: CA587570195
Gene:

Linked Data

ClinVar Variation Id: 551723
ClinVar RCV Id: RCV000666857 RCV000809273
dbSNP Id: rs1554651413
gnomAD v2: 9-35658017-C-CGTCCTCAGCTTCACAGAGTAGTA
gnomAD v3: 9-35658020-C-CGTCCTCAGCTTCACAGAGTAGTA
gnomAD v4: 9-35658020-C-CGTCCTCAGCTTCACAGAGTAGTA
MyVariant Identifiers: chr9:g.35658017_35658018insGTCCTCAGCTTCACAGAGTAGTA (hg19) chr9:g.35658021_35658043dup (hg38) chr9:g.35658020_35658021insGTCCTCAGCTTCACAGAGTAGTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658021_35658043dup , CM000671.2:g.35658021_35658043dup GRCh38
NC_000009.11:g.35658018_35658040dup , CM000671.1:g.35658018_35658040dup GRCh37
NC_000009.10:g.35648018_35648040dup NCBI36
NG_017041.1:g.4976_4998dup , LRG_163:g.4976_4998dup
NG_033120.1:g.4732_4754dup
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