Canonical Allele Identifier: CA437335041
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs1270908140

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712417G>T , CM000665.2:g.181712417G>T GRCh38
NC_000003.11:g.181430205G>T , CM000665.1:g.181430205G>T GRCh37
NC_000003.10:g.182912899G>T NCBI36
NG_009080.1:g.5484G>T , LRG_719:g.5484G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325404.3:c.57G>T (SOX2) MANE Select ENSP00000323588.1:p.Gly19=
ENST00000325404.2:c.57G>T (SOX2) ENSP00000323588.1:p.Gly19=
NM_003106.3:c.57G>T (SOX2) NP_003097.1:p.Gly19=
NR_004053.3:n.768-2768G>T (SOX2-OT)
NR_075089.1:n.767+12534G>T (SOX2-OT)
NR_075090.1:n.482-27152G>T (SOX2-OT)
NR_075091.1:n.783-2768G>T (SOX2-OT)
NR_075092.1:n.782+12534G>T (SOX2-OT)
NR_075093.1:n.473-27152G>T (SOX2-OT)
NM_003106.4:c.57G>T (SOX2) MANE Select NP_003097.1:p.Gly19=