HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50915890del , CM000685.2:g.50915890del | GRCh38 |
NC_000023.10:g.50658890del , CM000685.1:g.50658890del | GRCh37 |
NC_000023.9:g.50675630del | NCBI36 |
NG_012894.1:g.10107del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252677.4:c.462del MANE Select | ENSP00000252677.3:p.Trp155GlyfsTer22 | |
ENST00000252677.3:c.462del | ENSP00000252677.3:p.Trp155GlyfsTer22 | |
NM_005448.2:c.462del MANE Select | NP_005439.2:p.Trp155GlyfsTer22 |