HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129531778T= , CM000665.2:g.129531778T= | GRCh38 |
NC_000003.11:g.129250621T= , CM000665.1:g.129250621T= | GRCh37 |
NC_000003.10:g.130733311T= | NCBI36 |
NG_009115.1:g.8140T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.531-473T= MANE Select | ENSP00000296271.3:n.531-473T= | |
ENST00000296271.3:c.531-473T= | ENSP00000296271.3:n.531-473T= | |
NM_000539.3:c.531-473T= MANE Select | NP_000530.1:n.531-473T= |