Canonical Allele Identifier: CA345865950
Gene: SOX11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.5832963G>C (hg19) chr2:g.5692831G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692831G>C , CM000664.2:g.5692831G>C GRCh38
NC_000002.11:g.5832963G>C , CM000664.1:g.5832963G>C GRCh37
NC_000002.10:g.5750414G>C NCBI36
NG_050751.1:g.5165G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.110G>C MANE Select ENSP00000322568.3:p.Ser37Thr
ENST00000322002.4:c.110G>C ENSP00000322568.3:p.Ser37Thr
NM_003108.3:c.110G>C NP_003099.1:p.Ser37Thr
NM_003108.4:c.110G>C MANE Select NP_003099.1:p.Ser37Thr
Search 100 bp 5'
Search 100 bp 3'