HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189098780T= , CM000664.2:g.189098780T= | GRCh38 |
NC_000002.11:g.189963506T= , CM000664.1:g.189963506T= | GRCh37 |
NC_000002.10:g.189671751T= | NCBI36 |
NG_011799.1:g.86100A= | |
NG_011799.2:g.86100A= | |
NG_011799.3:g.131522A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.370-21A= MANE Select | ENSP00000364000.3:n.370-21A= | |
ENST00000649966.1:c.232-21A= | ENSP00000496785.1:n.232-21A= | |
ENST00000374866.7:c.370-21A= | ENSP00000364000.3:n.370-21A= | |
ENST00000618828.1:c.-261-21A= | ENSP00000482184.1:n.-261-21A= | |
NM_000393.3:c.370-21A= | NP_000384.2:n.370-21A= | |
XM_011510573.1:c.232-21A= | XP_011508875.1:n.232-21A= | |
NM_000393.4:c.370-21A= | NP_000384.2:n.370-21A= | |
XM_011510573.3:c.232-21A= | XP_011508875.1:n.232-21A= | |
NM_000393.5:c.370-21A= MANE Select | NP_000384.2:n.370-21A= |