HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181712951G>C , CM000665.2:g.181712951G>C | GRCh38 |
NC_000003.11:g.181430739G>C , CM000665.1:g.181430739G>C | GRCh37 |
NC_000003.10:g.182913433G>C | NCBI36 |
NG_009080.1:g.6018G>C , LRG_719:g.6018G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.591G>C (SOX2) MANE Select | ENSP00000323588.1:p.Met197Ile | |
ENST00000325404.2:c.591G>C (SOX2) | ENSP00000323588.1:p.Met197Ile | |
NM_003106.3:c.591G>C (SOX2) | NP_003097.1:p.Met197Ile | |
NR_004053.3:n.768-2234G>C (SOX2-OT) | ||
NR_075089.1:n.767+13068G>C (SOX2-OT) | ||
NR_075090.1:n.482-26618G>C (SOX2-OT) | ||
NR_075091.1:n.783-2234G>C (SOX2-OT) | ||
NR_075092.1:n.782+13068G>C (SOX2-OT) | ||
NR_075093.1:n.473-26618G>C (SOX2-OT) | ||
NM_003106.4:c.591G>C (SOX2) MANE Select | NP_003097.1:p.Met197Ile |