Canonical Allele Identifier: CA345866098

Gene: SOX11

Linked Data

• MyVariant Identifiers: chr2:g.5833024G>A (hg19) ; chr2:g.5692892G>A (hg38)

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