Canonical Allele Identifier: CA1424778979
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712434C= , CM000665.2:g.181712434C= GRCh38
NC_000003.11:g.181430222C= , CM000665.1:g.181430222C= GRCh37
NC_000003.10:g.182912916C= NCBI36
NG_009080.1:g.5501C= , LRG_719:g.5501C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.74C= (SOX2) MANE Select ENSP00000323588.1:p.Ser25=
ENST00000325404.2:c.74C= (SOX2) ENSP00000323588.1:p.Ser25=
NM_003106.3:c.74C= (SOX2) NP_003097.1:p.Ser25=
NR_004053.3:n.768-2751C= (SOX2-OT)
NR_075089.1:n.767+12551C= (SOX2-OT)
NR_075090.1:n.482-27135C= (SOX2-OT)
NR_075091.1:n.783-2751C= (SOX2-OT)
NR_075092.1:n.782+12551C= (SOX2-OT)
NR_075093.1:n.473-27135C= (SOX2-OT)
NM_003106.4:c.74C= (SOX2) MANE Select NP_003097.1:p.Ser25=
Search 100 bp 5'
Search 100 bp 3'