HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189098688A= , CM000664.2:g.189098688A= | GRCh38 |
NC_000002.11:g.189963414A= , CM000664.1:g.189963414A= | GRCh37 |
NC_000002.10:g.189671659A= | NCBI36 |
NG_011799.1:g.86192T= | |
NG_011799.2:g.86192T= | |
NG_011799.3:g.131614T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.402+39T= MANE Select | ENSP00000364000.3:n.402+39T= | |
ENST00000649966.1:c.264+39T= | ENSP00000496785.1:n.264+39T= | |
ENST00000374866.7:c.402+39T= | ENSP00000364000.3:n.402+39T= | |
ENST00000618828.1:c.-229+39T= | ENSP00000482184.1:n.-229+39T= | |
NM_000393.3:c.402+39T= | NP_000384.2:n.402+39T= | |
XM_011510573.1:c.264+39T= | XP_011508875.1:n.264+39T= | |
NM_000393.4:c.402+39T= | NP_000384.2:n.402+39T= | |
XM_011510573.3:c.264+39T= | XP_011508875.1:n.264+39T= | |
NM_000393.5:c.402+39T= MANE Select | NP_000384.2:n.402+39T= |