HGVS | Genome Assembly |
---|---|
NC_000010.11:g.68231500del , CM000672.2:g.68231500del | GRCh38 |
NC_000010.10:g.69991257del , CM000672.1:g.69991257del | GRCh37 |
NC_000010.9:g.69661263del | NCBI36 |
NG_031934.1:g.5615del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373673.5:c.179del MANE Select | ENSP00000362777.3:p.Phe60SerfsTer27 | |
ENST00000373673.4:c.179del | ENSP00000362777.3:p.Phe60SerfsTer27 | |
NM_145178.3:c.179del | NP_660161.1:p.Phe60SerfsTer27 | |
NM_145178.4:c.179del MANE Select | NP_660161.1:p.Phe60SerfsTer27 |