Canonical Allele Identifier: CA2273926357
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123597C= , CM000679.2:g.72123597C= GRCh38
NC_000017.10:g.70119738C= , CM000679.1:g.70119738C= GRCh37
NC_000017.9:g.67631333C= NCBI36
NG_012490.1:g.7578C=

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.740C= MANE Select ENSP00000245479.2:p.Pro247=
ENST00000245479.2:c.740C= ENSP00000245479.2:p.Pro247=
NM_000346.3:c.740C= NP_000337.1:p.Pro247=
NM_000346.4:c.740C= MANE Select NP_000337.1:p.Pro247=