Canonical Allele Identifier: CA1424780887
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713788G= , CM000665.2:g.181713788G= GRCh38
NC_000003.11:g.181431576G= , CM000665.1:g.181431576G= GRCh37
NC_000003.10:g.182914270G= NCBI36
NG_009080.1:g.6855G= , LRG_719:g.6855G=

Transcript Alleles

HGVS Amino-acid change
ENST00000325404.3:c.*474G= (SOX2) MANE Select ENSP00000323588.1:n.*474G=
ENST00000325404.2:c.*474G= (SOX2) ENSP00000323588.1:n.*474G=
NM_003106.3:c.*474G= (SOX2) NP_003097.1:n.*474G=
NR_004053.3:n.768-1397G= (SOX2-OT)
NR_075089.1:n.767+13905G= (SOX2-OT)
NR_075090.1:n.482-25781G= (SOX2-OT)
NR_075091.1:n.783-1397G= (SOX2-OT)
NR_075092.1:n.782+13905G= (SOX2-OT)
NR_075093.1:n.473-25781G= (SOX2-OT)
NM_003106.4:c.*474G= (SOX2) MANE Select NP_003097.1:n.*474G=