Canonical Allele Identifier: CA1424780665
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713573A= , CM000665.2:g.181713573A= GRCh38
NC_000003.11:g.181431361A= , CM000665.1:g.181431361A= GRCh37
NC_000003.10:g.182914055A= NCBI36
NG_009080.1:g.6640A= , LRG_719:g.6640A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*259A= (SOX2) MANE Select ENSP00000323588.1:n.*259A=
ENST00000325404.2:c.*259A= (SOX2) ENSP00000323588.1:n.*259A=
NM_003106.3:c.*259A= (SOX2) NP_003097.1:n.*259A=
NR_004053.3:n.768-1612A= (SOX2-OT)
NR_075089.1:n.767+13690A= (SOX2-OT)
NR_075090.1:n.482-25996A= (SOX2-OT)
NR_075091.1:n.783-1612A= (SOX2-OT)
NR_075092.1:n.782+13690A= (SOX2-OT)
NR_075093.1:n.473-25996A= (SOX2-OT)
NM_003106.4:c.*259A= (SOX2) MANE Select NP_003097.1:n.*259A=
Search 100 bp 5'
Search 100 bp 3'