Canonical Allele Identifier: CA355473555
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs2108522069

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712652C>G , CM000665.2:g.181712652C>G GRCh38
NC_000003.11:g.181430440C>G , CM000665.1:g.181430440C>G GRCh37
NC_000003.10:g.182913134C>G NCBI36
NG_009080.1:g.5719C>G , LRG_719:g.5719C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.292C>G (SOX2) MANE Select ENSP00000323588.1:p.Arg98Gly
ENST00000325404.2:c.292C>G (SOX2) ENSP00000323588.1:p.Arg98Gly
NM_003106.3:c.292C>G (SOX2) NP_003097.1:p.Arg98Gly
NR_004053.3:n.768-2533C>G (SOX2-OT)
NR_075089.1:n.767+12769C>G (SOX2-OT)
NR_075090.1:n.482-26917C>G (SOX2-OT)
NR_075091.1:n.783-2533C>G (SOX2-OT)
NR_075092.1:n.782+12769C>G (SOX2-OT)
NR_075093.1:n.473-26917C>G (SOX2-OT)
NM_003106.4:c.292C>G (SOX2) MANE Select NP_003097.1:p.Arg98Gly