Canonical Allele Identifier: CA345865869

Gene: SOX11

Linked Data

• MyVariant Identifiers: chr2:g.5832929T>A (hg19) ; chr2:g.5692797T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.5692797T>A , CM000664.2:g.5692797T>A	GRCh38
NC_000002.11:g.5832929T>A , CM000664.1:g.5832929T>A	GRCh37
NC_000002.10:g.5750380T>A	NCBI36
NG_050751.1:g.5131T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322002.5:c.76T>A MANE Select	ENSP00000322568.3:p.Phe26Ile
ENST00000322002.4:c.76T>A	ENSP00000322568.3:p.Phe26Ile
NM_003108.3:c.76T>A	NP_003099.1:p.Phe26Ile
NM_003108.4:c.76T>A MANE Select	NP_003099.1:p.Phe26Ile