HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43172119C>A , CM000683.2:g.43172119C>A | GRCh38 |
NG_009823.1:g.8089C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291554.6:c.361C>A MANE Select | ENSP00000291554.2:p.Pro121Thr | |
ENST00000398132.1:c.250C>A | ENSP00000381200.1:p.Pro84Thr | |
ENST00000398133.5:c.301C>A | ENSP00000381201.1:p.Pro101Thr | |
ENST00000468016.1:n.462C>A | ||
ENST00000482775.1:n.442C>A | ||
NM_000394.3:c.361C>A | NP_000385.1:p.Pro121Thr | |
XM_005261093.2:c.250C>A | XP_005261150.1:p.Pro84Thr | |
NM_001363766.1:c.250C>A | NP_001350695.1:p.Pro84Thr | |
NM_000394.4:c.361C>A MANE Select | NP_000385.1:p.Pro121Thr |