HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43172117T>G , CM000683.2:g.43172117T>G | GRCh38 |
NG_009823.1:g.8087T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291554.6:c.359T>G MANE Select | ENSP00000291554.2:p.Leu120Arg | |
ENST00000398132.1:c.248T>G | ENSP00000381200.1:p.Leu83Arg | |
ENST00000398133.5:c.299T>G | ENSP00000381201.1:p.Leu100Arg | |
ENST00000468016.1:n.460T>G | ||
ENST00000482775.1:n.440T>G | ||
NM_000394.3:c.359T>G | NP_000385.1:p.Leu120Arg | |
XM_005261093.2:c.248T>G | XP_005261150.1:p.Leu83Arg | |
NM_001363766.1:c.248T>G | NP_001350695.1:p.Leu83Arg | |
NM_000394.4:c.359T>G MANE Select | NP_000385.1:p.Leu120Arg |