Canonical Allele Identifier: CA355474285
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712980A>G , CM000665.2:g.181712980A>G GRCh38
NC_000003.11:g.181430768A>G , CM000665.1:g.181430768A>G GRCh37
NC_000003.10:g.182913462A>G NCBI36
NG_009080.1:g.6047A>G , LRG_719:g.6047A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.620A>G (SOX2) MANE Select ENSP00000323588.1:p.Tyr207Cys
ENST00000325404.2:c.620A>G (SOX2) ENSP00000323588.1:p.Tyr207Cys
NM_003106.3:c.620A>G (SOX2) NP_003097.1:p.Tyr207Cys
NR_004053.3:n.768-2205A>G (SOX2-OT)
NR_075089.1:n.767+13097A>G (SOX2-OT)
NR_075090.1:n.482-26589A>G (SOX2-OT)
NR_075091.1:n.783-2205A>G (SOX2-OT)
NR_075092.1:n.782+13097A>G (SOX2-OT)
NR_075093.1:n.473-26589A>G (SOX2-OT)
NM_003106.4:c.620A>G (SOX2) MANE Select NP_003097.1:p.Tyr207Cys