Canonical Allele Identifier: CA437335549
Gene: SOX2 HGNC NCBI
SOX2-OT HGNC NCBI

Linked Data

dbSNP Id: rs1222809271
MyVariant Identifiers: chr3:g.181430721A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.181712933A>C , CM000665.2:g.181712933A>C GRCh38
NC_000003.11:g.181430721A>C , CM000665.1:g.181430721A>C GRCh37
NC_000003.10:g.182913415A>C NCBI36
NG_009080.1:g.6000A>C , LRG_719:g.6000A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325404.3:c.573A>C (SOX2) MANE Select ENSP00000323588.1:p.Ala191=
ENST00000325404.2:c.573A>C (SOX2) ENSP00000323588.1:p.Ala191=
NM_003106.3:c.573A>C (SOX2) NP_003097.1:p.Ala191=
NR_004053.3:n.768-2252A>C (SOX2-OT)
NR_075089.1:n.767+13050A>C (SOX2-OT)
NR_075090.1:n.482-26636A>C (SOX2-OT)
NR_075091.1:n.783-2252A>C (SOX2-OT)
NR_075092.1:n.782+13050A>C (SOX2-OT)
NR_075093.1:n.473-26636A>C (SOX2-OT)
NM_003106.4:c.573A>C (SOX2) MANE Select NP_003097.1:p.Ala191=