HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44287033T>A , CM000683.2:g.44287033T>A | GRCh38 |
NC_000021.8:g.45706916T>A , CM000683.1:g.45706916T>A | GRCh37 |
NC_000021.7:g.44531344T>A | NCBI36 |
NG_009556.1:g.6154T>A , LRG_18:g.6154T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.363T>A MANE Select | ENSP00000291582.5:p.Ala121= | |
ENST00000291582.5:c.363T>A | ENSP00000291582.5:p.Ala121= | |
ENST00000527919.5:n.524T>A | ||
ENST00000530812.5:n.532T>A | ||
NM_000383.3:c.363T>A | NP_000374.1:p.Ala121= | |
XM_011529551.1:c.363T>A | XP_011527853.1:p.Ala121= | |
NM_000383.4:c.363T>A MANE Select | NP_000374.1:p.Ala121= |