HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189098710T= , CM000664.2:g.189098710T= | GRCh38 |
NC_000002.11:g.189963436T= , CM000664.1:g.189963436T= | GRCh37 |
NC_000002.10:g.189671681T= | NCBI36 |
NG_011799.1:g.86170A= | |
NG_011799.2:g.86170A= | |
NG_011799.3:g.131592A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.402+17A= MANE Select | ENSP00000364000.3:n.402+17A= | |
ENST00000649966.1:c.264+17A= | ENSP00000496785.1:n.264+17A= | |
ENST00000374866.7:c.402+17A= | ENSP00000364000.3:n.402+17A= | |
ENST00000618828.1:c.-229+17A= | ENSP00000482184.1:n.-229+17A= | |
NM_000393.3:c.402+17A= | NP_000384.2:n.402+17A= | |
XM_011510573.1:c.264+17A= | XP_011508875.1:n.264+17A= | |
NM_000393.4:c.402+17A= | NP_000384.2:n.402+17A= | |
XM_011510573.3:c.264+17A= | XP_011508875.1:n.264+17A= | |
NM_000393.5:c.402+17A= MANE Select | NP_000384.2:n.402+17A= |