HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169541024G= , CM000663.2:g.169541024G= | GRCh38 |
NC_000001.10:g.169510262G= , CM000663.1:g.169510262G= | GRCh37 |
NC_000001.9:g.167776886G= | NCBI36 |
NG_011806.1:g.50508C= , LRG_553:g.50508C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.4066C= MANE Select | ENSP00000356771.3:p.Pro1356= | |
ENST00000367796.3:c.4081C= | ENSP00000356770.3:p.Pro1361= | |
ENST00000367797.7:c.4066C= | ENSP00000356771.3:p.Pro1356= | |
NM_000130.4:c.4066C= , LRG_553t1:c.4066C= | NP_000121.2:p.Pro1356= | |
XM_017000660.2:c.3655C= | XP_016856149.1:p.Pro1219= | |
NM_000130.5:c.4066C= MANE Select | NP_000121.2:p.Pro1356= |