HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270261T= , CM000668.2:g.31270261T= | GRCh38 |
NC_000006.11:g.31238038T= , CM000668.1:g.31238038T= | GRCh37 |
NC_000006.10:g.31346017T= | NCBI36 |
NG_029422.2:g.6871A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.844A= MANE Select | ENSP00000365402.5:p.Thr282= | |
ENST00000376228.9:c.844A= | ENSP00000365402.5:p.Thr282= | |
ENST00000376237.8:c.*431A= | ENSP00000365412.4:n.*431A= | |
ENST00000383329.7:c.844A= | ENSP00000372819.3:p.Thr282= | |
ENST00000415537.1:c.735A= | ||
ENST00000470363.5:n.162A= | ||
ENST00000487245.5:n.1203A= | ||
ENST00000495835.1:n.1033A= | ||
NM_002117.5:c.844A= | NP_002108.4:p.Thr282= | |
NM_002117.6:c.844A= MANE Select | NP_002108.4:p.Thr282= |