Canonical Allele Identifier: CA400866620
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1390665178

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122876C>A , CM000679.2:g.72122876C>A GRCh38
NC_000017.10:g.70119017C>A , CM000679.1:g.70119017C>A GRCh37
NC_000017.9:g.67630612C>A NCBI36
NG_012490.1:g.6857C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.589C>A MANE Select ENSP00000245479.2:p.His197Asn
ENST00000245479.2:c.589C>A ENSP00000245479.2:p.His197Asn
NM_000346.3:c.589C>A NP_000337.1:p.His197Asn
NM_000346.4:c.589C>A MANE Select NP_000337.1:p.His197Asn