HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42687913C= , CM000679.2:g.42687913C= | GRCh38 |
NC_000017.10:g.40839931C= , CM000679.1:g.40839931C= | GRCh37 |
NC_000017.9:g.38093457C= | NCBI36 |
NG_042091.1:g.10300C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264638.9:c.1238C= MANE Select | ENSP00000264638.3:p.Thr413= | |
ENST00000264638.8:c.1238C= | ENSP00000264638.3:p.Thr413= | |
ENST00000586801.1:n.653C= | ||
ENST00000591662.1:c.1238C= | ENSP00000466571.1:p.Thr413= | |
NM_003632.2:c.1238C= | NP_003623.1:p.Thr413= | |
XM_005257748.3:c.1010C= | XP_005257805.1:p.Thr337= | |
XM_005257748.4:c.1010C= | XP_005257805.1:p.Thr337= | |
XM_017025238.1:c.1238C= | XP_016880727.1:p.Thr413= | |
XM_024451011.1:c.1238C= | XP_024306779.1:p.Thr413= | |
NM_003632.3:c.1238C= MANE Select | NP_003623.1:p.Thr413= |