Canonical Allele Identifier: CA400867800
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs267605028

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124001C>G , CM000679.2:g.72124001C>G GRCh38
NC_000017.10:g.70120142C>G , CM000679.1:g.70120142C>G GRCh37
NC_000017.9:g.67631737C>G NCBI36
NG_012490.1:g.7982C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1144C>G MANE Select ENSP00000245479.2:p.Leu382Val
ENST00000245479.2:c.1144C>G ENSP00000245479.2:p.Leu382Val
NM_000346.3:c.1144C>G NP_000337.1:p.Leu382Val
NM_000346.4:c.1144C>G MANE Select NP_000337.1:p.Leu382Val