HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181713068T>A , CM000665.2:g.181713068T>A | GRCh38 |
NC_000003.11:g.181430856T>A , CM000665.1:g.181430856T>A | GRCh37 |
NC_000003.10:g.182913550T>A | NCBI36 |
NG_009080.1:g.6135T>A , LRG_719:g.6135T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.708T>A (SOX2) MANE Select | ENSP00000323588.1:p.Ala236= | |
ENST00000325404.2:c.708T>A (SOX2) | ENSP00000323588.1:p.Ala236= | |
NM_003106.3:c.708T>A (SOX2) | NP_003097.1:p.Ala236= | |
NR_004053.3:n.768-2117T>A (SOX2-OT) | ||
NR_075089.1:n.767+13185T>A (SOX2-OT) | ||
NR_075090.1:n.482-26501T>A (SOX2-OT) | ||
NR_075091.1:n.783-2117T>A (SOX2-OT) | ||
NR_075092.1:n.782+13185T>A (SOX2-OT) | ||
NR_075093.1:n.473-26501T>A (SOX2-OT) | ||
NM_003106.4:c.708T>A (SOX2) MANE Select | NP_003097.1:p.Ala236= |