Canonical Allele Identifier: CA345865869
Gene: SOX11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.5832929T>A (hg19) chr2:g.5692797T>A (hg38)
JSON-LD

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
Search 100 bp 5'
Search 100 bp 3'