Canonical Allele Identifier: CA355475013
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713311G>C , CM000665.2:g.181713311G>C GRCh38
NC_000003.11:g.181431099G>C , CM000665.1:g.181431099G>C GRCh37
NC_000003.10:g.182913793G>C NCBI36
NG_009080.1:g.6378G>C , LRG_719:g.6378G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.951G>C (SOX2) MANE Select ENSP00000323588.1:p.Met317Ile
ENST00000325404.2:c.951G>C (SOX2) ENSP00000323588.1:p.Met317Ile
NM_003106.3:c.951G>C (SOX2) NP_003097.1:p.Met317Ile
NR_004053.3:n.768-1874G>C (SOX2-OT)
NR_075089.1:n.767+13428G>C (SOX2-OT)
NR_075090.1:n.482-26258G>C (SOX2-OT)
NR_075091.1:n.783-1874G>C (SOX2-OT)
NR_075092.1:n.782+13428G>C (SOX2-OT)
NR_075093.1:n.473-26258G>C (SOX2-OT)
NM_003106.4:c.951G>C (SOX2) MANE Select NP_003097.1:p.Met317Ile