HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181713346T= , CM000665.2:g.181713346T= | GRCh38 |
NC_000003.11:g.181431134T= , CM000665.1:g.181431134T= | GRCh37 |
NC_000003.10:g.182913828T= | NCBI36 |
NG_009080.1:g.6413T= , LRG_719:g.6413T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.*32T= (SOX2) MANE Select | ENSP00000323588.1:n.*32T= | |
ENST00000325404.2:c.*32T= (SOX2) | ENSP00000323588.1:n.*32T= | |
NM_003106.3:c.*32T= (SOX2) | NP_003097.1:n.*32T= | |
NR_004053.3:n.768-1839T= (SOX2-OT) | ||
NR_075089.1:n.767+13463T= (SOX2-OT) | ||
NR_075090.1:n.482-26223T= (SOX2-OT) | ||
NR_075091.1:n.783-1839T= (SOX2-OT) | ||
NR_075092.1:n.782+13463T= (SOX2-OT) | ||
NR_075093.1:n.473-26223T= (SOX2-OT) | ||
NM_003106.4:c.*32T= (SOX2) MANE Select | NP_003097.1:n.*32T= |