HGVS | Genome Assembly |
---|---|
NC_000012.12:g.76346899T>A , CM000674.2:g.76346899T>A | GRCh38 |
NC_000012.11:g.76740679T>A , CM000674.1:g.76740679T>A | GRCh37 |
NC_000012.10:g.75264810T>A | NCBI36 |
NG_016357.1:g.6544A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650064.2:c.1086A>T MANE Select | ENSP00000497413.1:p.Ile362= | |
ENST00000393262.3:c.1086A>T | ENSP00000376946.3:p.Ile362= | |
NM_024685.3:c.1086A>T | NP_078961.3:p.Ile362= | |
NM_024685.4:c.1086A>T MANE Select | NP_078961.3:p.Ile362= |