Canonical Allele Identifier:
CA863578605
Gene:
Linked Data
ClinVar Variation Id:
1446490
ClinVar RCV Id:
RCV001992855
dbSNP Id:
rs1218494857
MyVariant Identifiers:
chr9:g.35658015_35658016insACGTTCTCAGCTTT (hg19)
chr9:g.35658018_35658019insACGTTCTCAGCTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35658022_35658023insTCTCAGCTTTACGT , CM000671.2:g.35658022_35658023insTCTCAGCTTTACGT | GRCh38 |
| NC_000009.11:g.35658019_35658020insTCTCAGCTTTACGT , CM000671.1:g.35658019_35658020insTCTCAGCTTTACGT | GRCh37 |
| NC_000009.10:g.35648019_35648020insTCTCAGCTTTACGT | NCBI36 |
| NG_017041.1:g.5000_5001insAAAGCTGAGAACGT , LRG_163:g.5000_5001insAAAGCTGAGAACGT | |
| NG_033120.1:g.4733_4734insTCTCAGCTTTACGT |