Canonical Allele Identifier: CA400866339
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs965946174
MyVariant Identifiers: chr17:g.70118886C>A (hg19) chr17:g.72122745C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122745C>A , CM000679.2:g.72122745C>A GRCh38
NC_000017.10:g.70118886C>A , CM000679.1:g.70118886C>A GRCh37
NC_000017.9:g.67630481C>A NCBI36
NG_012490.1:g.6726C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.458C>A MANE Select ENSP00000245479.2:p.Pro153His
ENST00000245479.2:c.458C>A ENSP00000245479.2:p.Pro153His
NM_000346.3:c.458C>A NP_000337.1:p.Pro153His
NM_000346.4:c.458C>A MANE Select NP_000337.1:p.Pro153His
Search 100 bp 5'
Search 100 bp 3'