HGVS | Genome Assembly |
---|---|
NC_000003.12:g.98391569del , CM000665.2:g.98391569del | GRCh38 |
NC_000003.11:g.98110413del , CM000665.1:g.98110413del | GRCh37 |
NC_000003.10:g.99593103del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000383695.1:c.904del MANE Select | ENSP00000373194.1:p.Ile302LeufsTer2 | |
NM_001005516.1:c.904del MANE Select | NP_001005516.1:p.Ile302LeufsTer2 |