HGVS | Genome Assembly |
---|---|
NC_000003.12:g.180659681G= , CM000665.2:g.180659681G= | GRCh38 |
NC_000003.11:g.180377469G= , CM000665.1:g.180377469G= | GRCh37 |
NC_000003.10:g.181860163G= | NCBI36 |
NG_029581.1:g.24815C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000476379.6:c.605C= MANE Select | ENSP00000417960.2:p.Ala202= | |
ENST00000650641.1:n.684C= | ||
ENST00000650889.1:n.777C= | ||
ENST00000651046.1:c.605C= | ENSP00000499175.1:p.Ala202= | |
ENST00000651818.1:n.747C= | ||
ENST00000652024.1:n.696C= | ||
ENST00000652408.1:n.742C= | ||
ENST00000442201.6:c.605C= | ENSP00000405708.2:p.Ala202= | |
ENST00000476379.5:c.605C= | ENSP00000417960.1:p.Ala202= | |
NM_181426.1:c.605C= | NP_852091.1:p.Ala202= | |
NM_181426.2:c.605C= MANE Select | NP_852091.1:p.Ala202= |