Canonical Allele Identifier: CA400866968
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143250706

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123606C>T , CM000679.2:g.72123606C>T GRCh38
NC_000017.10:g.70119747C>T , CM000679.1:g.70119747C>T GRCh37
NC_000017.9:g.67631342C>T NCBI36
NG_012490.1:g.7587C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.749C>T MANE Select ENSP00000245479.2:p.Ala250Val
ENST00000245479.2:c.749C>T ENSP00000245479.2:p.Ala250Val
NM_000346.3:c.749C>T NP_000337.1:p.Ala250Val
NM_000346.4:c.749C>T MANE Select NP_000337.1:p.Ala250Val