HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189050674A>T , CM000664.2:g.189050674A>T | GRCh38 |
NC_000002.11:g.189915400A>T , CM000664.1:g.189915400A>T | GRCh37 |
NC_000002.10:g.189623645A>T | NCBI36 |
NG_011799.1:g.134206T>A | |
NG_011799.2:g.134206T>A | |
NG_011799.3:g.179628T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.2934T>A MANE Select | ENSP00000364000.3:p.Gly978= | |
ENST00000374866.7:c.2934T>A | ENSP00000364000.3:p.Gly978= | |
ENST00000618828.1:c.1773T>A | ENSP00000482184.1:p.Gly591= | |
NM_000393.3:c.2934T>A | NP_000384.2:p.Gly978= | |
XM_011510573.1:c.2796T>A | XP_011508875.1:p.Gly932= | |
NM_000393.4:c.2934T>A | NP_000384.2:p.Gly978= | |
XM_011510573.3:c.2796T>A | XP_011508875.1:p.Gly932= | |
NM_000393.5:c.2934T>A MANE Select | NP_000384.2:p.Gly978= |