HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181712611A>C , CM000665.2:g.181712611A>C | GRCh38 |
NC_000003.11:g.181430399A>C , CM000665.1:g.181430399A>C | GRCh37 |
NC_000003.10:g.182913093A>C | NCBI36 |
NG_009080.1:g.5678A>C , LRG_719:g.5678A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.251A>C (SOX2) MANE Select | ENSP00000323588.1:p.Glu84Ala | |
ENST00000325404.2:c.251A>C (SOX2) | ENSP00000323588.1:p.Glu84Ala | |
NM_003106.3:c.251A>C (SOX2) | NP_003097.1:p.Glu84Ala | |
NR_004053.3:n.768-2574A>C (SOX2-OT) | ||
NR_075089.1:n.767+12728A>C (SOX2-OT) | ||
NR_075090.1:n.482-26958A>C (SOX2-OT) | ||
NR_075091.1:n.783-2574A>C (SOX2-OT) | ||
NR_075092.1:n.782+12728A>C (SOX2-OT) | ||
NR_075093.1:n.473-26958A>C (SOX2-OT) | ||
NM_003106.4:c.251A>C (SOX2) MANE Select | NP_003097.1:p.Glu84Ala |