Canonical Allele Identifier: CA437335049
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs2108521440
MyVariant Identifiers: chr3:g.181430214C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712426C>A , CM000665.2:g.181712426C>A GRCh38
NC_000003.11:g.181430214C>A , CM000665.1:g.181430214C>A GRCh37
NC_000003.10:g.182912908C>A NCBI36
NG_009080.1:g.5493C>A , LRG_719:g.5493C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325404.3:c.66C>A (SOX2) MANE Select ENSP00000323588.1:p.Gly22=
ENST00000325404.2:c.66C>A (SOX2) ENSP00000323588.1:p.Gly22=
NM_003106.3:c.66C>A (SOX2) NP_003097.1:p.Gly22=
NR_004053.3:n.768-2759C>A (SOX2-OT)
NR_075089.1:n.767+12543C>A (SOX2-OT)
NR_075090.1:n.482-27143C>A (SOX2-OT)
NR_075091.1:n.783-2759C>A (SOX2-OT)
NR_075092.1:n.782+12543C>A (SOX2-OT)
NR_075093.1:n.473-27143C>A (SOX2-OT)
NM_003106.4:c.66C>A (SOX2) MANE Select NP_003097.1:p.Gly22=