HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65029547T>A , CM000677.2:g.65029547T>A | GRCh38 |
NC_000015.9:g.65321885T>A , CM000677.1:g.65321885T>A | GRCh37 |
NC_000015.8:g.63108938T>A | NCBI36 |
NG_029184.1:g.5093A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000220058.9:c.67A>T MANE Select | ENSP00000220058.4:p.Ser23Cys | |
ENST00000220058.8:c.67A>T | ENSP00000220058.4:p.Ser23Cys | |
ENST00000543678.1:c.67A>T | ENSP00000443754.1:p.Ser23Cys | |
ENST00000558460.5:c.67A>T | ENSP00000452646.1:p.Ser23Cys | |
ENST00000558614.1:n.28A>T | ||
ENST00000560717.5:c.52A>T | ENSP00000457257.1:p.Ser18Cys | |
NM_139242.3:c.67A>T | NP_640335.2:p.Ser23Cys | |
XM_005254158.5:c.67A>T | XP_005254215.2:p.Ser23Cys | |
XR_001751081.1:n.82A>T | ||
NM_139242.4:c.67A>T MANE Select | NP_640335.2:p.Ser23Cys |