Canonical Allele Identifier: CA1424779849
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713027T= , CM000665.2:g.181713027T= GRCh38
NC_000003.11:g.181430815T= , CM000665.1:g.181430815T= GRCh37
NC_000003.10:g.182913509T= NCBI36
NG_009080.1:g.6094T= , LRG_719:g.6094T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.667T= (SOX2) MANE Select ENSP00000323588.1:p.Tyr223=
ENST00000325404.2:c.667T= (SOX2) ENSP00000323588.1:p.Tyr223=
NM_003106.3:c.667T= (SOX2) NP_003097.1:p.Tyr223=
NR_004053.3:n.768-2158T= (SOX2-OT)
NR_075089.1:n.767+13144T= (SOX2-OT)
NR_075090.1:n.482-26542T= (SOX2-OT)
NR_075091.1:n.783-2158T= (SOX2-OT)
NR_075092.1:n.782+13144T= (SOX2-OT)
NR_075093.1:n.473-26542T= (SOX2-OT)
NM_003106.4:c.667T= (SOX2) MANE Select NP_003097.1:p.Tyr223=