Canonical Allele Identifier: CA8739120
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs375976801

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124042G>A , CM000679.2:g.72124042G>A GRCh38
NC_000017.10:g.70120183G>A , CM000679.1:g.70120183G>A GRCh37
NC_000017.9:g.67631778G>A NCBI36
NG_012490.1:g.8023G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1185G>A MANE Select ENSP00000245479.2:p.Thr395=
ENST00000245479.2:c.1185G>A ENSP00000245479.2:p.Thr395=
NM_000346.3:c.1185G>A NP_000337.1:p.Thr395=
NM_000346.4:c.1185G>A MANE Select NP_000337.1:p.Thr395=