Canonical Allele Identifier: CA424762821
Gene: SOX11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.5833453G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5693321G>A , CM000664.2:g.5693321G>A GRCh38
NC_000002.11:g.5833453G>A , CM000664.1:g.5833453G>A GRCh37
NC_000002.10:g.5750904G>A NCBI36
NG_050751.1:g.5655G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322002.5:c.600G>A MANE Select ENSP00000322568.3:p.Leu200=
ENST00000322002.4:c.600G>A ENSP00000322568.3:p.Leu200=
NM_003108.3:c.600G>A NP_003099.1:p.Leu200=
NM_003108.4:c.600G>A MANE Select NP_003099.1:p.Leu200=
Search 100 bp 5'
Search 100 bp 3'