Linked Data
ClinVar Variation Id:
7321
ClinVar RCV Id:
RCV000007745
dbSNP Id:
rs199476393
MyVariant Identifiers:
chr3:g.169482741_169482742delinsCT (hg19)
chr3:g.169764953_169764954delinsCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169764953_169764954delinsCT , CM000665.2:g.169764953_169764954delinsCT | GRCh38 |
| NC_000003.11:g.169482741_169482742delinsCT , CM000665.1:g.169482741_169482742delinsCT | GRCh37 |
| NC_000003.10:g.170965435_170965436delinsCT | NCBI36 |
| NG_016363.1:g.5107_5108delinsAG , LRG_347:g.5107_5108delinsAG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_001566.1:n.107_108delinsAG , LRG_347t1:n.107_108delinsAG |