Canonical Allele Identifier: CA587570189
Gene:

Linked Data

ClinVar Variation Id: 556339
ClinVar RCV Id: RCV000672334 RCV003758905
dbSNP Id: rs1554651397
gnomAD v2: 9-35658015-C-CACGTCCTCAGCTTCACAGAGTT
gnomAD v4: 9-35658018-C-CACGTCCTCAGCTTCACAGAGTT
MyVariant Identifiers: chr9:g.35658015_35658016insACGTCCTCAGCTTCACAGAGTT (hg19) chr9:g.35658018_35658019insACGTCCTCAGCTTCACAGAGTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658039_35658040insTACGTCCTCAGCTTCACAGAGT , CM000671.2:g.35658039_35658040insTACGTCCTCAGCTTCACAGAGT GRCh38
NC_000009.11:g.35658036_35658037insTACGTCCTCAGCTTCACAGAGT , CM000671.1:g.35658036_35658037insTACGTCCTCAGCTTCACAGAGT GRCh37
NC_000009.10:g.35648036_35648037insTACGTCCTCAGCTTCACAGAGT NCBI36
NG_017041.1:g.5000_5001insAACTCTGTGAAGCTGAGGACGT , LRG_163:g.5000_5001insAACTCTGTGAAGCTGAGGACGT
NG_033120.1:g.4750_4751insTACGTCCTCAGCTTCACAGAGT
Search 100 bp 5'
Search 100 bp 3'