HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52451632del , CM000674.2:g.52451632del | GRCh38 |
NC_000012.11:g.52845416del , CM000674.1:g.52845416del | GRCh37 |
NC_000012.10:g.51131683del | NCBI36 |
NG_008299.1:g.5496del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252252.4:c.448del MANE Select | ENSP00000252252.3:p.Leu150CysfsTer? | |
ENST00000252252.3:c.448del | ENSP00000252252.3:p.Leu150CysfsTer? | |
NM_005555.3:c.448del | NP_005546.2:p.Leu150CysfsTer? | |
NM_005555.4:c.448del MANE Select | NP_005546.2:p.Leu150CysfsTer? |