Canonical Allele Identifier: CA400866944
Gene: SOX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123595G>T , CM000679.2:g.72123595G>T GRCh38
NC_000017.10:g.70119736G>T , CM000679.1:g.70119736G>T GRCh37
NC_000017.9:g.67631331G>T NCBI36
NG_012490.1:g.7576G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.738G>T MANE Select ENSP00000245479.2:p.Gln246His
ENST00000245479.2:c.738G>T ENSP00000245479.2:p.Gln246His
NM_000346.3:c.738G>T NP_000337.1:p.Gln246His
NM_000346.4:c.738G>T MANE Select NP_000337.1:p.Gln246His