HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33068756C>A , CM000668.2:g.33068756C>A | GRCh38 |
NC_000006.11:g.33036533C>A , CM000668.1:g.33036533C>A | GRCh37 |
NC_000006.10:g.33144511C>A | NCBI36 |
NG_033241.1:g.17023G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000692443.1:c.677G>T MANE Select | ENSP00000509163.1:p.Cys226Phe | |
ENST00000419277.5:c.677G>T | ENSP00000393566.1:p.Cys226Phe | |
ENST00000437811.1:c.279G>T | ||
ENST00000479107.1:n.1276G>T | ||
NM_001242524.1:c.677G>T | NP_001229453.1:p.Cys226Phe | |
NM_001242525.1:c.677G>T | NP_001229454.1:p.Cys226Phe | |
NM_033554.3:c.677G>T | NP_291032.2:p.Cys226Phe | |
XM_011514559.1:c.628+263G>T | XP_011512861.1:n.628+263G>T | |
NM_001242524.2:c.677G>T | NP_001229453.1:p.Cys226Phe | |
NM_001242525.2:c.677G>T | NP_001229454.1:p.Cys226Phe |