Canonical Allele Identifier: CA1424780675
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713577T= , CM000665.2:g.181713577T= GRCh38
NC_000003.11:g.181431365T= , CM000665.1:g.181431365T= GRCh37
NC_000003.10:g.182914059T= NCBI36
NG_009080.1:g.6644T= , LRG_719:g.6644T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*263T= (SOX2) MANE Select ENSP00000323588.1:n.*263T=
ENST00000325404.2:c.*263T= (SOX2) ENSP00000323588.1:n.*263T=
NM_003106.3:c.*263T= (SOX2) NP_003097.1:n.*263T=
NR_004053.3:n.768-1608T= (SOX2-OT)
NR_075089.1:n.767+13694T= (SOX2-OT)
NR_075090.1:n.482-25992T= (SOX2-OT)
NR_075091.1:n.783-1608T= (SOX2-OT)
NR_075092.1:n.782+13694T= (SOX2-OT)
NR_075093.1:n.473-25992T= (SOX2-OT)
NM_003106.4:c.*263T= (SOX2) MANE Select NP_003097.1:n.*263T=