Canonical Allele Identifier: CA355473058
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs2108521451
MyVariant Identifiers: chr3:g.181430219A>C (hg19) chr3:g.181712431A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712431A>C , CM000665.2:g.181712431A>C GRCh38
NC_000003.11:g.181430219A>C , CM000665.1:g.181430219A>C GRCh37
NC_000003.10:g.182912913A>C NCBI36
NG_009080.1:g.5498A>C , LRG_719:g.5498A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325404.3:c.71A>C (SOX2) MANE Select ENSP00000323588.1:p.Asn24Thr
ENST00000325404.2:c.71A>C (SOX2) ENSP00000323588.1:p.Asn24Thr
NM_003106.3:c.71A>C (SOX2) NP_003097.1:p.Asn24Thr
NR_004053.3:n.768-2754A>C (SOX2-OT)
NR_075089.1:n.767+12548A>C (SOX2-OT)
NR_075090.1:n.482-27138A>C (SOX2-OT)
NR_075091.1:n.783-2754A>C (SOX2-OT)
NR_075092.1:n.782+12548A>C (SOX2-OT)
NR_075093.1:n.473-27138A>C (SOX2-OT)
NM_003106.4:c.71A>C (SOX2) MANE Select NP_003097.1:p.Asn24Thr
Search 100 bp 5'
Search 100 bp 3'