Canonical Allele Identifier: CA400868300
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs764925787
MyVariant Identifiers: chr17:g.70120365C>A (hg19) chr17:g.72124224C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124224C>A , CM000679.2:g.72124224C>A GRCh38
NC_000017.10:g.70120365C>A , CM000679.1:g.70120365C>A GRCh37
NC_000017.9:g.67631960C>A NCBI36
NG_012490.1:g.8205C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1367C>A MANE Select ENSP00000245479.2:p.Ala456Glu
ENST00000245479.2:c.1367C>A ENSP00000245479.2:p.Ala456Glu
NM_000346.3:c.1367C>A NP_000337.1:p.Ala456Glu
NM_000346.4:c.1367C>A MANE Select NP_000337.1:p.Ala456Glu
Search 100 bp 5'
Search 100 bp 3'