Canonical Allele Identifier: CA587570199
Gene:

Linked Data

ClinVar Variation Id: 1065911
ClinVar RCV Id: RCV001376761
dbSNP Id: rs1563907859
gnomAD v2: 9-35658018-G-GTCCTCAGCTTCACAGA
gnomAD v4: 9-35658021-G-GTCCTCAGCTTCACAGA
MyVariant Identifiers: chr9:g.35658018_35658019insTCCTCAGCTTCACAGA (hg19) chr9:g.35658021_35658022insTCCTCAGCTTCACAGA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658022_35658037dup , CM000671.2:g.35658022_35658037dup GRCh38
NC_000009.11:g.35658019_35658034dup , CM000671.1:g.35658019_35658034dup GRCh37
NC_000009.10:g.35648019_35648034dup NCBI36
NG_017041.1:g.4982_4997dup , LRG_163:g.4982_4997dup
NG_033120.1:g.4733_4748dup
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