HGVS | Genome Assembly |
---|---|
NC_000003.12:g.180659498A>T , CM000665.2:g.180659498A>T | GRCh38 |
NC_000003.11:g.180377286A>T , CM000665.1:g.180377286A>T | GRCh37 |
NC_000003.10:g.181859980A>T | NCBI36 |
NG_029581.1:g.24998T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000476379.6:c.692T>A MANE Select | ENSP00000417960.2:p.Ile231Lys | |
ENST00000650641.1:n.771T>A | ||
ENST00000650889.1:n.864T>A | ||
ENST00000651046.1:c.692T>A | ENSP00000499175.1:p.Ile231Lys | |
ENST00000651818.1:n.834T>A | ||
ENST00000652024.1:n.783T>A | ||
ENST00000652408.1:n.829T>A | ||
ENST00000442201.6:c.692T>A | ENSP00000405708.2:p.Ile231Lys | |
ENST00000476379.5:c.692T>A | ENSP00000417960.1:p.Ile231Lys | |
NM_181426.1:c.692T>A | NP_852091.1:p.Ile231Lys | |
NM_181426.2:c.692T>A MANE Select | NP_852091.1:p.Ile231Lys |