HGVS | Genome Assembly |
---|---|
NC_000003.12:g.180659551A>T , CM000665.2:g.180659551A>T | GRCh38 |
NC_000003.11:g.180377339A>T , CM000665.1:g.180377339A>T | GRCh37 |
NC_000003.10:g.181860033A>T | NCBI36 |
NG_029581.1:g.24945T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000476379.6:c.639T>A MANE Select | ENSP00000417960.2:p.Phe213Leu | |
ENST00000650641.1:n.718T>A | ||
ENST00000650889.1:n.811T>A | ||
ENST00000651046.1:c.639T>A | ENSP00000499175.1:p.Phe213Leu | |
ENST00000651818.1:n.781T>A | ||
ENST00000652024.1:n.730T>A | ||
ENST00000652408.1:n.776T>A | ||
ENST00000442201.6:c.639T>A | ENSP00000405708.2:p.Phe213Leu | |
ENST00000476379.5:c.639T>A | ENSP00000417960.1:p.Phe213Leu | |
NM_181426.1:c.639T>A | NP_852091.1:p.Phe213Leu | |
NM_181426.2:c.639T>A MANE Select | NP_852091.1:p.Phe213Leu |