Canonical Allele Identifier: CA400866958
Gene: SOX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123602A>T , CM000679.2:g.72123602A>T GRCh38
NC_000017.10:g.70119743A>T , CM000679.1:g.70119743A>T GRCh37
NC_000017.9:g.67631338A>T NCBI36
NG_012490.1:g.7583A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.745A>T MANE Select ENSP00000245479.2:p.Lys249Ter
ENST00000245479.2:c.745A>T ENSP00000245479.2:p.Lys249Ter
NM_000346.3:c.745A>T NP_000337.1:p.Lys249Ter
NM_000346.4:c.745A>T MANE Select NP_000337.1:p.Lys249Ter