HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181713569G>T , CM000665.2:g.181713569G>T | GRCh38 |
NC_000003.11:g.181431357G>T , CM000665.1:g.181431357G>T | GRCh37 |
NC_000003.10:g.182914051G>T | NCBI36 |
NG_009080.1:g.6636G>T , LRG_719:g.6636G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.*255G>T (SOX2) MANE Select | ENSP00000323588.1:n.*255G>T | |
ENST00000325404.2:c.*255G>T (SOX2) | ENSP00000323588.1:n.*255G>T | |
NM_003106.3:c.*255G>T (SOX2) | NP_003097.1:n.*255G>T | |
NR_004053.3:n.768-1616G>T (SOX2-OT) | ||
NR_075089.1:n.767+13686G>T (SOX2-OT) | ||
NR_075090.1:n.482-26000G>T (SOX2-OT) | ||
NR_075091.1:n.783-1616G>T (SOX2-OT) | ||
NR_075092.1:n.782+13686G>T (SOX2-OT) | ||
NR_075093.1:n.473-26000G>T (SOX2-OT) | ||
NM_003106.4:c.*255G>T (SOX2) MANE Select | NP_003097.1:n.*255G>T |