Canonical Allele Identifier: CA345865872
Gene: SOX11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.5832930T>G (hg19) chr2:g.5692798T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692798T>G , CM000664.2:g.5692798T>G GRCh38
NC_000002.11:g.5832930T>G , CM000664.1:g.5832930T>G GRCh37
NC_000002.10:g.5750381T>G NCBI36
NG_050751.1:g.5132T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.77T>G MANE Select ENSP00000322568.3:p.Phe26Cys
ENST00000322002.4:c.77T>G ENSP00000322568.3:p.Phe26Cys
NM_003108.3:c.77T>G NP_003099.1:p.Phe26Cys
NM_003108.4:c.77T>G MANE Select NP_003099.1:p.Phe26Cys
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