HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64160108T= , CM000677.2:g.64160108T= | GRCh38 |
NC_000015.9:g.64452307T= , CM000677.1:g.64452307T= | GRCh37 |
NC_000015.8:g.62239360T= | NCBI36 |
NG_012979.1:g.8048A= , LRG_10:g.8048A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000300026.4:c.339A= MANE Select | ENSP00000300026.4:p.Thr113= | |
ENST00000561048.2:n.372A= | ||
ENST00000680158.1:c.339A= | ENSP00000504873.1:p.Thr113= | |
ENST00000680343.1:n.293A= | ||
ENST00000681397.1:c.339A= | ENSP00000506584.1:p.Thr113= | |
ENST00000681658.1:c.234A= | ENSP00000505431.1:p.Thr78= | |
ENST00000300026.3:c.339A= | ENSP00000300026.3:p.Thr113= | |
ENST00000558492.1:n.245A= | ||
ENST00000561048.1:n.374A= | ||
NM_000942.4:c.339A= , LRG_10t1:c.339A= | NP_000933.1:p.Thr113= | |
NM_000942.5:c.339A= MANE Select | NP_000933.1:p.Thr113= |