Canonical Allele Identifier: CA355474213
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712950T>C , CM000665.2:g.181712950T>C GRCh38
NC_000003.11:g.181430738T>C , CM000665.1:g.181430738T>C GRCh37
NC_000003.10:g.182913432T>C NCBI36
NG_009080.1:g.6017T>C , LRG_719:g.6017T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.590T>C (SOX2) MANE Select ENSP00000323588.1:p.Met197Thr
ENST00000325404.2:c.590T>C (SOX2) ENSP00000323588.1:p.Met197Thr
NM_003106.3:c.590T>C (SOX2) NP_003097.1:p.Met197Thr
NR_004053.3:n.768-2235T>C (SOX2-OT)
NR_075089.1:n.767+13067T>C (SOX2-OT)
NR_075090.1:n.482-26619T>C (SOX2-OT)
NR_075091.1:n.783-2235T>C (SOX2-OT)
NR_075092.1:n.782+13067T>C (SOX2-OT)
NR_075093.1:n.473-26619T>C (SOX2-OT)
NM_003106.4:c.590T>C (SOX2) MANE Select NP_003097.1:p.Met197Thr