Canonical Allele Identifier: CA8739154
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs566738702

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124234C>T , CM000679.2:g.72124234C>T GRCh38
NC_000017.10:g.70120375C>T , CM000679.1:g.70120375C>T GRCh37
NC_000017.9:g.67631970C>T NCBI36
NG_012490.1:g.8215C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1377C>T MANE Select ENSP00000245479.2:p.Gly459=
ENST00000245479.2:c.1377C>T ENSP00000245479.2:p.Gly459=
NM_000346.3:c.1377C>T NP_000337.1:p.Gly459=
NM_000346.4:c.1377C>T MANE Select NP_000337.1:p.Gly459=