HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68646864del , CM000666.2:g.68646864del | GRCh38 |
NC_000004.11:g.69512582del , CM000666.1:g.69512582del | GRCh37 |
NC_000004.10:g.69195177del | NCBI36 |
NG_052676.1:g.28913del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.*240del MANE Select | ENSP00000341045.5:n.*240del | |
ENST00000338206.5:c.*240del | ENSP00000341045.5:n.*240del | |
ENST00000616841.4:c.1732+101del | ENSP00000482004.1:n.1732+101del | |
NM_001076.3:c.*240del | NP_001067.2:n.*240del | |
NM_001076.4:c.*240del MANE Select | NP_001067.2:n.*240del |