Canonical Allele Identifier: CA587570186
Gene:

Linked Data

ClinVar Variation Id: 2981551
ClinVar RCV Id: RCV003835173
dbSNP Id: rs1554651379
gnomAD v2: 9-35658014-C-CCACGTCCTCAGCTTCACAGAGTAGTA
MyVariant Identifiers: chr9:g.35658014_35658015insCACGTCCTCAGCTTCACAGAGTAGTA (hg19) chr9:g.35658017_35658018insCACGTCCTCAGCTTCACAGAGTAGTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658018_35658043dup , CM000671.2:g.35658018_35658043dup GRCh38
NC_000009.11:g.35658015_35658040dup , CM000671.1:g.35658015_35658040dup GRCh37
NC_000009.10:g.35648015_35648040dup NCBI36
NG_017041.1:g.4976_5001dup , LRG_163:g.4976_5001dup
NG_033120.1:g.4729_4754dup
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