Canonical Allele Identifier: CA1235671320
Gene: SOX11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692807G= , CM000664.2:g.5692807G= GRCh38
NC_000002.11:g.5832939G= , CM000664.1:g.5832939G= GRCh37
NC_000002.10:g.5750390G= NCBI36
NG_050751.1:g.5141G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.86G= MANE Select ENSP00000322568.3:p.Cys29=
ENST00000322002.4:c.86G= ENSP00000322568.3:p.Cys29=
NM_003108.3:c.86G= NP_003099.1:p.Cys29=
NM_003108.4:c.86G= MANE Select NP_003099.1:p.Cys29=
Search 100 bp 5'
Search 100 bp 3'