Canonical Allele Identifier: CA437335213

Gene: SOX2 SOX2-OT

Linked Data

• dbSNP Id: rs2108522093
• MyVariant Identifiers: chr3:g.181430445G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.181712657G>C , CM000665.2:g.181712657G>C	GRCh38
NC_000003.11:g.181430445G>C , CM000665.1:g.181430445G>C	GRCh37
NC_000003.10:g.182913139G>C	NCBI36
NG_009080.1:g.5724G>C , LRG_719:g.5724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325404.3:c.297G>C (SOX2) MANE Select	ENSP00000323588.1:p.Ala99=
ENST00000325404.2:c.297G>C (SOX2)	ENSP00000323588.1:p.Ala99=
NM_003106.3:c.297G>C (SOX2)	NP_003097.1:p.Ala99=
NR_004053.3:n.768-2528G>C (SOX2-OT)
NR_075089.1:n.767+12774G>C (SOX2-OT)
NR_075090.1:n.482-26912G>C (SOX2-OT)
NR_075091.1:n.783-2528G>C (SOX2-OT)
NR_075092.1:n.782+12774G>C (SOX2-OT)
NR_075093.1:n.473-26912G>C (SOX2-OT)
NM_003106.4:c.297G>C (SOX2) MANE Select	NP_003097.1:p.Ala99=