Canonical Allele Identifier: CA424762889
Gene: SOX11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.5832994C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692862C>A , CM000664.2:g.5692862C>A GRCh38
NC_000002.11:g.5832994C>A , CM000664.1:g.5832994C>A GRCh37
NC_000002.10:g.5750445C>A NCBI36
NG_050751.1:g.5196C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.141C>A MANE Select ENSP00000322568.3:p.Gly47=
ENST00000322002.4:c.141C>A ENSP00000322568.3:p.Gly47=
NM_003108.3:c.141C>A NP_003099.1:p.Gly47=
NM_003108.4:c.141C>A MANE Select NP_003099.1:p.Gly47=
Search 100 bp 5'
Search 100 bp 3'