Canonical Allele Identifier: CA400867556
Gene: SOX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.70120022C>A (hg19) chr17:g.72123881C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123881C>A , CM000679.2:g.72123881C>A GRCh38
NC_000017.10:g.70120022C>A , CM000679.1:g.70120022C>A GRCh37
NC_000017.9:g.67631617C>A NCBI36
NG_012490.1:g.7862C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1024C>A MANE Select ENSP00000245479.2:p.Pro342Thr
ENST00000245479.2:c.1024C>A ENSP00000245479.2:p.Pro342Thr
NM_000346.3:c.1024C>A NP_000337.1:p.Pro342Thr
NM_000346.4:c.1024C>A MANE Select NP_000337.1:p.Pro342Thr
Search 100 bp 5'
Search 100 bp 3'