Canonical Allele Identifier: CA400866946
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs566929141

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123596C>G , CM000679.2:g.72123596C>G GRCh38
NC_000017.10:g.70119737C>G , CM000679.1:g.70119737C>G GRCh37
NC_000017.9:g.67631332C>G NCBI36
NG_012490.1:g.7577C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.739C>G MANE Select ENSP00000245479.2:p.Pro247Ala
ENST00000245479.2:c.739C>G ENSP00000245479.2:p.Pro247Ala
NM_000346.3:c.739C>G NP_000337.1:p.Pro247Ala
NM_000346.4:c.739C>G MANE Select NP_000337.1:p.Pro247Ala