Canonical Allele Identifier: CA400866872
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143250161
COSMIC: COSM473290
MyVariant Identifiers: chr17:g.70119701C>G (hg19) chr17:g.72123560C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123560C>G , CM000679.2:g.72123560C>G GRCh38
NC_000017.10:g.70119701C>G , CM000679.1:g.70119701C>G GRCh37
NC_000017.9:g.67631296C>G NCBI36
NG_012490.1:g.7541C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.703C>G MANE Select ENSP00000245479.2:p.Pro235Ala
ENST00000245479.2:c.703C>G ENSP00000245479.2:p.Pro235Ala
NM_000346.3:c.703C>G NP_000337.1:p.Pro235Ala
NM_000346.4:c.703C>G MANE Select NP_000337.1:p.Pro235Ala
Search 100 bp 5'
Search 100 bp 3'