ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.169765034_169765035insG , CM000665.2:g.169765034_169765035insG | GRCh38 |
| NC_000003.11:g.169482822_169482823insG , CM000665.1:g.169482822_169482823insG | GRCh37 |
| NC_000003.10:g.170965516_170965517insG | NCBI36 |
| NG_016363.1:g.5026_5027insC , LRG_347:g.5026_5027insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_001566.1:n.26_27insC , LRG_347t1:n.26_27insC |