Canonical Allele Identifier: CA400867701
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1201663893

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123951C>T , CM000679.2:g.72123951C>T GRCh38
NC_000017.10:g.70120092C>T , CM000679.1:g.70120092C>T GRCh37
NC_000017.9:g.67631687C>T NCBI36
NG_012490.1:g.7932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1094C>T MANE Select ENSP00000245479.2:p.Ala365Val
ENST00000245479.2:c.1094C>T ENSP00000245479.2:p.Ala365Val
NM_000346.3:c.1094C>T NP_000337.1:p.Ala365Val
NM_000346.4:c.1094C>T MANE Select NP_000337.1:p.Ala365Val