HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52451627del , CM000674.2:g.52451627del | GRCh38 |
NC_000012.11:g.52845411del , CM000674.1:g.52845411del | GRCh37 |
NC_000012.10:g.51131678del | NCBI36 |
NG_008299.1:g.5502del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252252.4:c.454del MANE Select | ENSP00000252252.3:p.Ile152LeufsTer? | |
ENST00000252252.3:c.454del | ENSP00000252252.3:p.Ile152LeufsTer? | |
NM_005555.3:c.454del | NP_005546.2:p.Ile152LeufsTer? | |
NM_005555.4:c.454del MANE Select | NP_005546.2:p.Ile152LeufsTer? |