Canonical Allele Identifier: CA1057047414
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs1714909660

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713788G>A , CM000665.2:g.181713788G>A GRCh38
NC_000003.11:g.181431576G>A , CM000665.1:g.181431576G>A GRCh37
NC_000003.10:g.182914270G>A NCBI36
NG_009080.1:g.6855G>A , LRG_719:g.6855G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325404.3:c.*474G>A (SOX2) MANE Select ENSP00000323588.1:n.*474G>A
ENST00000325404.2:c.*474G>A (SOX2) ENSP00000323588.1:n.*474G>A
NM_003106.3:c.*474G>A (SOX2) NP_003097.1:n.*474G>A
NR_004053.3:n.768-1397G>A (SOX2-OT)
NR_075089.1:n.767+13905G>A (SOX2-OT)
NR_075090.1:n.482-25781G>A (SOX2-OT)
NR_075091.1:n.783-1397G>A (SOX2-OT)
NR_075092.1:n.782+13905G>A (SOX2-OT)
NR_075093.1:n.473-25781G>A (SOX2-OT)
NM_003106.4:c.*474G>A (SOX2) MANE Select NP_003097.1:n.*474G>A