HGVS | Genome Assembly |
---|---|
NC_000003.12:g.42688197G>T , CM000665.2:g.42688197G>T | GRCh38 |
NC_000003.11:g.42729689G>T , CM000665.1:g.42729689G>T | GRCh37 |
NC_000003.10:g.42704693G>T | NCBI36 |
NG_033035.1:g.7679G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287777.5:c.1208G>T MANE Select | ENSP00000287777.4:p.Cys403Phe | |
ENST00000287777.4:c.1208G>T | ENSP00000287777.4:p.Cys403Phe | |
NM_152393.3:c.1208G>T | NP_689606.2:p.Cys403Phe | |
XM_005264866.2:c.1208G>T | XP_005264923.1:p.Cys403Phe | |
NM_152393.4:c.1208G>T MANE Select | NP_689606.2:p.Cys403Phe |