HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181712500C>G , CM000665.2:g.181712500C>G | GRCh38 |
NC_000003.11:g.181430288C>G , CM000665.1:g.181430288C>G | GRCh37 |
NC_000003.10:g.182912982C>G | NCBI36 |
NG_009080.1:g.5567C>G , LRG_719:g.5567C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.140C>G (SOX2) MANE Select | ENSP00000323588.1:p.Ala47Gly | |
ENST00000325404.2:c.140C>G (SOX2) | ENSP00000323588.1:p.Ala47Gly | |
NM_003106.3:c.140C>G (SOX2) | NP_003097.1:p.Ala47Gly | |
NR_004053.3:n.768-2685C>G (SOX2-OT) | ||
NR_075089.1:n.767+12617C>G (SOX2-OT) | ||
NR_075090.1:n.482-27069C>G (SOX2-OT) | ||
NR_075091.1:n.783-2685C>G (SOX2-OT) | ||
NR_075092.1:n.782+12617C>G (SOX2-OT) | ||
NR_075093.1:n.473-27069C>G (SOX2-OT) | ||
NM_003106.4:c.140C>G (SOX2) MANE Select | NP_003097.1:p.Ala47Gly |