Canonical Allele Identifier: CA501432716
Gene: SOX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.70120063C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123922C>A , CM000679.2:g.72123922C>A GRCh38
NC_000017.10:g.70120063C>A , CM000679.1:g.70120063C>A GRCh37
NC_000017.9:g.67631658C>A NCBI36
NG_012490.1:g.7903C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1065C>A MANE Select ENSP00000245479.2:p.Ala355=
ENST00000245479.2:c.1065C>A ENSP00000245479.2:p.Ala355=
NM_000346.3:c.1065C>A NP_000337.1:p.Ala355=
NM_000346.4:c.1065C>A MANE Select NP_000337.1:p.Ala355=
Search 100 bp 5'
Search 100 bp 3'