Canonical Allele Identifier: CA1424779530
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712808G= , CM000665.2:g.181712808G= GRCh38
NC_000003.11:g.181430596G= , CM000665.1:g.181430596G= GRCh37
NC_000003.10:g.182913290G= NCBI36
NG_009080.1:g.5875G= , LRG_719:g.5875G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.448G= (SOX2) MANE Select ENSP00000323588.1:p.Gly150=
ENST00000325404.2:c.448G= (SOX2) ENSP00000323588.1:p.Gly150=
NM_003106.3:c.448G= (SOX2) NP_003097.1:p.Gly150=
NR_004053.3:n.768-2377G= (SOX2-OT)
NR_075089.1:n.767+12925G= (SOX2-OT)
NR_075090.1:n.482-26761G= (SOX2-OT)
NR_075091.1:n.783-2377G= (SOX2-OT)
NR_075092.1:n.782+12925G= (SOX2-OT)
NR_075093.1:n.473-26761G= (SOX2-OT)
NM_003106.4:c.448G= (SOX2) MANE Select NP_003097.1:p.Gly150=