HGVS | Genome Assembly |
---|---|
NC_000023.11:g.83508670del , CM000685.2:g.83508670del | GRCh38 |
NC_000023.10:g.82763678del , CM000685.1:g.82763678del | GRCh37 |
NC_000023.9:g.82650334del | NCBI36 |
NG_009936.2:g.5410del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644024.2:c.346del MANE Select | ENSP00000495996.1:p.Ala116ProfsTer26 | |
ENST00000373200.4:c.346del | ENSP00000362296.2:p.Ala116ProfsTer26 | |
NM_000307.4:c.346del | NP_000298.3:p.Ala116ProfsTer26 | |
NM_000307.5:c.346del MANE Select | NP_000298.3:p.Ala116ProfsTer26 |