HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189098727T>C , CM000664.2:g.189098727T>C | GRCh38 |
NC_000002.11:g.189963453T>C , CM000664.1:g.189963453T>C | GRCh37 |
NC_000002.10:g.189671698T>C | NCBI36 |
NG_011799.1:g.86153A>G | |
NG_011799.2:g.86153A>G | |
NG_011799.3:g.131575A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.402A>G MANE Select | ENSP00000364000.3:p.Ala134= | |
ENST00000649966.1:c.264A>G | ENSP00000496785.1:p.Ala88= | |
ENST00000374866.7:c.402A>G | ENSP00000364000.3:p.Ala134= | |
ENST00000618828.1:c.-229A>G | ENSP00000482184.1:n.-229A>G | |
NM_000393.3:c.402A>G | NP_000384.2:p.Ala134= | |
XM_011510573.1:c.264A>G | XP_011508875.1:p.Ala88= | |
NM_000393.4:c.402A>G | NP_000384.2:p.Ala134= | |
XM_011510573.3:c.264A>G | XP_011508875.1:p.Ala88= | |
NM_000393.5:c.402A>G MANE Select | NP_000384.2:p.Ala134= |