Canonical Allele Identifier: CA2273926361
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123604G= , CM000679.2:g.72123604G= GRCh38
NC_000017.10:g.70119745G= , CM000679.1:g.70119745G= GRCh37
NC_000017.9:g.67631340G= NCBI36
NG_012490.1:g.7585G=

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.747G= MANE Select ENSP00000245479.2:p.Lys249=
ENST00000245479.2:c.747G= ENSP00000245479.2:p.Lys249=
NM_000346.3:c.747G= NP_000337.1:p.Lys249=
NM_000346.4:c.747G= MANE Select NP_000337.1:p.Lys249=