HGVS | Genome Assembly |
---|---|
NC_000019.10:g.9126463_9126464insGAG , CM000681.2:g.9126463_9126464insGAG | GRCh38 |
NC_000019.9:g.9237139_9237140insGAG , CM000681.1:g.9237139_9237140insGAG | GRCh37 |
NC_000019.8:g.9098139_9098140insGAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305444.2:c.487_488insCTC MANE Select | ENSP00000302867.2:p.Val163delinsAlaLeu | |
NM_001001958.1:c.487_488insCTC MANE Select | NP_001001958.1:p.Val163delinsAlaLeu |