Canonical Allele Identifier: CA1057047304
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs1714903698

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713664T>A , CM000665.2:g.181713664T>A GRCh38
NC_000003.11:g.181431452T>A , CM000665.1:g.181431452T>A GRCh37
NC_000003.10:g.182914146T>A NCBI36
NG_009080.1:g.6731T>A , LRG_719:g.6731T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*350T>A (SOX2) MANE Select ENSP00000323588.1:n.*350T>A
ENST00000325404.2:c.*350T>A (SOX2) ENSP00000323588.1:n.*350T>A
NM_003106.3:c.*350T>A (SOX2) NP_003097.1:n.*350T>A
NR_004053.3:n.768-1521T>A (SOX2-OT)
NR_075089.1:n.767+13781T>A (SOX2-OT)
NR_075090.1:n.482-25905T>A (SOX2-OT)
NR_075091.1:n.783-1521T>A (SOX2-OT)
NR_075092.1:n.782+13781T>A (SOX2-OT)
NR_075093.1:n.473-25905T>A (SOX2-OT)
NM_003106.4:c.*350T>A (SOX2) MANE Select NP_003097.1:n.*350T>A