Canonical Allele Identifier: CA2273926709
Gene: SOX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124237C= , CM000679.2:g.72124237C= GRCh38
NC_000017.10:g.70120378C= , CM000679.1:g.70120378C= GRCh37
NC_000017.9:g.67631973C= NCBI36
NG_012490.1:g.8218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1380C= MANE Select ENSP00000245479.2:p.Thr460=
ENST00000245479.2:c.1380C= ENSP00000245479.2:p.Thr460=
NM_000346.3:c.1380C= NP_000337.1:p.Thr460=
NM_000346.4:c.1380C= MANE Select NP_000337.1:p.Thr460=
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