Canonical Allele Identifier: CA1424779768
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712948C= , CM000665.2:g.181712948C= GRCh38
NC_000003.11:g.181430736C= , CM000665.1:g.181430736C= GRCh37
NC_000003.10:g.182913430C= NCBI36
NG_009080.1:g.6015C= , LRG_719:g.6015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.588C= (SOX2) MANE Select ENSP00000323588.1:p.Pro196=
ENST00000325404.2:c.588C= (SOX2) ENSP00000323588.1:p.Pro196=
NM_003106.3:c.588C= (SOX2) NP_003097.1:p.Pro196=
NR_004053.3:n.768-2237C= (SOX2-OT)
NR_075089.1:n.767+13065C= (SOX2-OT)
NR_075090.1:n.482-26621C= (SOX2-OT)
NR_075091.1:n.783-2237C= (SOX2-OT)
NR_075092.1:n.782+13065C= (SOX2-OT)
NR_075093.1:n.473-26621C= (SOX2-OT)
NM_003106.4:c.588C= (SOX2) MANE Select NP_003097.1:p.Pro196=