Canonical Allele Identifier: CA400866948
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1460431767

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123597C>G , CM000679.2:g.72123597C>G GRCh38
NC_000017.10:g.70119738C>G , CM000679.1:g.70119738C>G GRCh37
NC_000017.9:g.67631333C>G NCBI36
NG_012490.1:g.7578C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.740C>G MANE Select ENSP00000245479.2:p.Pro247Arg
ENST00000245479.2:c.740C>G ENSP00000245479.2:p.Pro247Arg
NM_000346.3:c.740C>G NP_000337.1:p.Pro247Arg
NM_000346.4:c.740C>G MANE Select NP_000337.1:p.Pro247Arg