Canonical Allele Identifier: CA1424780391
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713319C= , CM000665.2:g.181713319C= GRCh38
NC_000003.11:g.181431107C= , CM000665.1:g.181431107C= GRCh37
NC_000003.10:g.182913801C= NCBI36
NG_009080.1:g.6386C= , LRG_719:g.6386C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*5C= (SOX2) MANE Select ENSP00000323588.1:n.*5C=
ENST00000325404.2:c.*5C= (SOX2) ENSP00000323588.1:n.*5C=
NM_003106.3:c.*5C= (SOX2) NP_003097.1:n.*5C=
NR_004053.3:n.768-1866C= (SOX2-OT)
NR_075089.1:n.767+13436C= (SOX2-OT)
NR_075090.1:n.482-26250C= (SOX2-OT)
NR_075091.1:n.783-1866C= (SOX2-OT)
NR_075092.1:n.782+13436C= (SOX2-OT)
NR_075093.1:n.473-26250C= (SOX2-OT)
NM_003106.4:c.*5C= (SOX2) MANE Select NP_003097.1:n.*5C=
Search 100 bp 5'
Search 100 bp 3'