HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169572266A>T , CM000663.2:g.169572266A>T | GRCh38 |
NC_000001.10:g.169541504A>T , CM000663.1:g.169541504A>T | GRCh37 |
NC_000001.9:g.167808128A>T | NCBI36 |
NG_011806.1:g.19266T>A , LRG_553:g.19266T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.328T>A MANE Select | ENSP00000356771.3:p.Leu110Met | |
ENST00000367796.3:c.328T>A | ENSP00000356770.3:p.Leu110Met | |
ENST00000367797.7:c.328T>A | ENSP00000356771.3:p.Leu110Met | |
NM_000130.4:c.328T>A , LRG_553t1:c.328T>A | NP_000121.2:p.Leu110Met | |
XM_017000660.2:c.-84T>A | XP_016856149.1:n.-84T>A | |
NM_000130.5:c.328T>A MANE Select | NP_000121.2:p.Leu110Met |