Canonical Allele Identifier: CA2273926562
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123954C= , CM000679.2:g.72123954C= GRCh38
NC_000017.10:g.70120095C= , CM000679.1:g.70120095C= GRCh37
NC_000017.9:g.67631690C= NCBI36
NG_012490.1:g.7935C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1097C= MANE Select ENSP00000245479.2:p.Pro366=
ENST00000245479.2:c.1097C= ENSP00000245479.2:p.Pro366=
NM_000346.3:c.1097C= NP_000337.1:p.Pro366=
NM_000346.4:c.1097C= MANE Select NP_000337.1:p.Pro366=