Canonical Allele Identifier: CA1424780466
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713381A= , CM000665.2:g.181713381A= GRCh38
NC_000003.11:g.181431169A= , CM000665.1:g.181431169A= GRCh37
NC_000003.10:g.182913863A= NCBI36
NG_009080.1:g.6448A= , LRG_719:g.6448A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*67A= (SOX2) MANE Select ENSP00000323588.1:n.*67A=
ENST00000325404.2:c.*67A= (SOX2) ENSP00000323588.1:n.*67A=
NM_003106.3:c.*67A= (SOX2) NP_003097.1:n.*67A=
NR_004053.3:n.768-1804A= (SOX2-OT)
NR_075089.1:n.767+13498A= (SOX2-OT)
NR_075090.1:n.482-26188A= (SOX2-OT)
NR_075091.1:n.783-1804A= (SOX2-OT)
NR_075092.1:n.782+13498A= (SOX2-OT)
NR_075093.1:n.473-26188A= (SOX2-OT)
NM_003106.4:c.*67A= (SOX2) MANE Select NP_003097.1:n.*67A=