Canonical Allele Identifier: CA8739037
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs761747688

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123695A>G , CM000679.2:g.72123695A>G GRCh38
NC_000017.10:g.70119836A>G , CM000679.1:g.70119836A>G GRCh37
NC_000017.9:g.67631431A>G NCBI36
NG_012490.1:g.7676A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.838A>G MANE Select ENSP00000245479.2:p.Ser280Gly
ENST00000245479.2:c.838A>G ENSP00000245479.2:p.Ser280Gly
NM_000346.3:c.838A>G NP_000337.1:p.Ser280Gly
NM_000346.4:c.838A>G MANE Select NP_000337.1:p.Ser280Gly