HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884716_149884717del , CM000663.2:g.149884716_149884717del | GRCh38 |
NC_000001.10:g.149856266_149856267del , CM000663.1:g.149856266_149856267del | GRCh37 |
NC_000001.9:g.148122890_148122891del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369155.4:c.*1543_*1544del MANE Select | ENSP00000358151.2:n.*1543_*1544del | |
ENST00000369155.3:c.*1543_*1544del | ENSP00000358151.2:n.*1543_*1544del | |
ENST00000369160.3:c.377+1547_377+1548del | ENSP00000375736.2:n.377+1547_377+1548del | |
NM_003528.2:c.*1543_*1544del | NP_003519.1:n.*1543_*1544del | |
NM_003528.3:c.*1543_*1544del MANE Select | NP_003519.1:n.*1543_*1544del |