Canonical Allele Identifier: CA345866207
Gene: SOX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.5692938G>A , CM000664.2:g.5692938G>A GRCh38
NC_000002.11:g.5833070G>A , CM000664.1:g.5833070G>A GRCh37
NC_000002.10:g.5750521G>A NCBI36
NG_050751.1:g.5272G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322002.5:c.217G>A MANE Select ENSP00000322568.3:p.Asp73Asn
ENST00000322002.4:c.217G>A ENSP00000322568.3:p.Asp73Asn
NM_003108.3:c.217G>A NP_003099.1:p.Asp73Asn
NM_003108.4:c.217G>A MANE Select NP_003099.1:p.Asp73Asn