Canonical Allele Identifier: CA355474417
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.181430824T>G (hg19) chr3:g.181713036T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181713036T>G , CM000665.2:g.181713036T>G GRCh38
NC_000003.11:g.181430824T>G , CM000665.1:g.181430824T>G GRCh37
NC_000003.10:g.182913518T>G NCBI36
NG_009080.1:g.6103T>G , LRG_719:g.6103T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.676T>G (SOX2) MANE Select ENSP00000323588.1:p.Ser226Ala
ENST00000325404.2:c.676T>G (SOX2) ENSP00000323588.1:p.Ser226Ala
NM_003106.3:c.676T>G (SOX2) NP_003097.1:p.Ser226Ala
NR_004053.3:n.768-2149T>G (SOX2-OT)
NR_075089.1:n.767+13153T>G (SOX2-OT)
NR_075090.1:n.482-26533T>G (SOX2-OT)
NR_075091.1:n.783-2149T>G (SOX2-OT)
NR_075092.1:n.782+13153T>G (SOX2-OT)
NR_075093.1:n.473-26533T>G (SOX2-OT)
NM_003106.4:c.676T>G (SOX2) MANE Select NP_003097.1:p.Ser226Ala
Search 100 bp 5'
Search 100 bp 3'