Canonical Allele Identifier: CA1424780538
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713480A= , CM000665.2:g.181713480A= GRCh38
NC_000003.11:g.181431268A= , CM000665.1:g.181431268A= GRCh37
NC_000003.10:g.182913962A= NCBI36
NG_009080.1:g.6547A= , LRG_719:g.6547A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.*166A= (SOX2) MANE Select ENSP00000323588.1:n.*166A=
ENST00000325404.2:c.*166A= (SOX2) ENSP00000323588.1:n.*166A=
NM_003106.3:c.*166A= (SOX2) NP_003097.1:n.*166A=
NR_004053.3:n.768-1705A= (SOX2-OT)
NR_075089.1:n.767+13597A= (SOX2-OT)
NR_075090.1:n.482-26089A= (SOX2-OT)
NR_075091.1:n.783-1705A= (SOX2-OT)
NR_075092.1:n.782+13597A= (SOX2-OT)
NR_075093.1:n.473-26089A= (SOX2-OT)
NM_003106.4:c.*166A= (SOX2) MANE Select NP_003097.1:n.*166A=