Canonical Allele Identifier: CA355473489
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712621G>C , CM000665.2:g.181712621G>C GRCh38
NC_000003.11:g.181430409G>C , CM000665.1:g.181430409G>C GRCh37
NC_000003.10:g.182913103G>C NCBI36
NG_009080.1:g.5688G>C , LRG_719:g.5688G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325404.3:c.261G>C (SOX2) MANE Select ENSP00000323588.1:p.Lys87Asn
ENST00000325404.2:c.261G>C (SOX2) ENSP00000323588.1:p.Lys87Asn
NM_003106.3:c.261G>C (SOX2) NP_003097.1:p.Lys87Asn
NR_004053.3:n.768-2564G>C (SOX2-OT)
NR_075089.1:n.767+12738G>C (SOX2-OT)
NR_075090.1:n.482-26948G>C (SOX2-OT)
NR_075091.1:n.783-2564G>C (SOX2-OT)
NR_075092.1:n.782+12738G>C (SOX2-OT)
NR_075093.1:n.473-26948G>C (SOX2-OT)
NM_003106.4:c.261G>C (SOX2) MANE Select NP_003097.1:p.Lys87Asn