HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181712423C>G , CM000665.2:g.181712423C>G | GRCh38 |
NC_000003.11:g.181430211C>G , CM000665.1:g.181430211C>G | GRCh37 |
NC_000003.10:g.182912905C>G | NCBI36 |
NG_009080.1:g.5490C>G , LRG_719:g.5490C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000325404.3:c.63C>G (SOX2) MANE Select | ENSP00000323588.1:p.Gly21= | |
ENST00000325404.2:c.63C>G (SOX2) | ENSP00000323588.1:p.Gly21= | |
NM_003106.3:c.63C>G (SOX2) | NP_003097.1:p.Gly21= | |
NR_004053.3:n.768-2762C>G (SOX2-OT) | ||
NR_075089.1:n.767+12540C>G (SOX2-OT) | ||
NR_075090.1:n.482-27146C>G (SOX2-OT) | ||
NR_075091.1:n.783-2762C>G (SOX2-OT) | ||
NR_075092.1:n.782+12540C>G (SOX2-OT) | ||
NR_075093.1:n.473-27146C>G (SOX2-OT) | ||
NM_003106.4:c.63C>G (SOX2) MANE Select | NP_003097.1:p.Gly21= |