Canonical Allele Identifier: CA345866098
Gene: SOX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692892G>A , CM000664.2:g.5692892G>A GRCh38
NC_000002.11:g.5833024G>A , CM000664.1:g.5833024G>A GRCh37
NC_000002.10:g.5750475G>A NCBI36
NG_050751.1:g.5226G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.171G>A MANE Select ENSP00000322568.3:p.Met57Ile
ENST00000322002.4:c.171G>A ENSP00000322568.3:p.Met57Ile
NM_003108.3:c.171G>A NP_003099.1:p.Met57Ile
NM_003108.4:c.171G>A MANE Select NP_003099.1:p.Met57Ile