HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129531043A= , CM000665.2:g.129531043A= | GRCh38 |
NC_000003.11:g.129249886A= , CM000665.1:g.129249886A= | GRCh37 |
NC_000003.10:g.130732576A= | NCBI36 |
NG_009115.1:g.7405A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296271.4:c.529A= MANE Select | ENSP00000296271.3:p.Arg177= | |
ENST00000296271.3:c.529A= | ENSP00000296271.3:p.Arg177= | |
NM_000539.3:c.529A= MANE Select | NP_000530.1:p.Arg177= |