Canonical Allele Identifier: CA587570187
Gene:

Linked Data

ClinVar Variation Id: 552761
ClinVar RCV Id: RCV000668083 RCV001245795
dbSNP Id: rs1554651396
gnomAD v2: 9-35658015-C-CACGTCCTCAGCTTCACAG
gnomAD v4: 9-35658018-C-CACGTCCTCAGCTTCACAG
MyVariant Identifiers: chr9:g.35658015_35658016insACGTCCTCAGCTTCACAG (hg19) chr9:g.35658019_35658036dup (hg38) chr9:g.35658018_35658019insACGTCCTCAGCTTCACAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658020_35658037dup , CM000671.2:g.35658020_35658037dup GRCh38
NC_000009.11:g.35658017_35658034dup , CM000671.1:g.35658017_35658034dup GRCh37
NC_000009.10:g.35648017_35648034dup NCBI36
NG_017041.1:g.4983_5000dup , LRG_163:g.4983_5000dup
NG_033120.1:g.4731_4748dup
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