Canonical Allele Identifier: CA345866046

Gene: SOX11

Linked Data

• MyVariant Identifiers: chr2:g.5833002A>G (hg19) ; chr2:g.5692870A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.5692870A>G , CM000664.2:g.5692870A>G	GRCh38
NC_000002.11:g.5833002A>G , CM000664.1:g.5833002A>G	GRCh37
NC_000002.10:g.5750453A>G	NCBI36
NG_050751.1:g.5204A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322002.5:c.149A>G MANE Select	ENSP00000322568.3:p.Lys50Arg
ENST00000322002.4:c.149A>G	ENSP00000322568.3:p.Lys50Arg
NM_003108.3:c.149A>G	NP_003099.1:p.Lys50Arg
NM_003108.4:c.149A>G MANE Select	NP_003099.1:p.Lys50Arg