HGVS | Genome Assembly |
---|---|
NC_000007.14:g.37888326G>A , CM000669.2:g.37888326G>A | GRCh38 |
NC_000007.13:g.37927928G>A , CM000669.1:g.37927928G>A | GRCh37 |
NC_000007.12:g.37894453G>A | NCBI36 |
NG_015893.1:g.44730G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000199447.9:c.1297G>A (NME8) MANE Select | ENSP00000199447.4:p.Gly433Ser | |
ENST00000199447.8:c.1297G>A (NME8) | ENSP00000199447.4:p.Gly433Ser | |
ENST00000426106.1:c.*243G>A (NME8) | ENSP00000408841.1:n.*243G>A | |
ENST00000440017.5:c.1297G>A (NME8) | ENSP00000397063.1:p.Gly433Ser | |
ENST00000476620.1:c.-38+30981G>A (EPDR1) | ENSP00000425858.1:n.-38+30981G>A | |
NM_016616.4:c.1297G>A (NME8) | NP_057700.3:p.Gly433Ser | |
NM_016616.5:c.1297G>A (NME8) MANE Select | NP_057700.3:p.Gly433Ser |