Canonical Allele Identifier: CA400868138
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1908209401
MyVariant Identifiers: chr17:g.70120293A>T (hg19) chr17:g.72124152A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124152A>T , CM000679.2:g.72124152A>T GRCh38
NC_000017.10:g.70120293A>T , CM000679.1:g.70120293A>T GRCh37
NC_000017.9:g.67631888A>T NCBI36
NG_012490.1:g.8133A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1295A>T MANE Select ENSP00000245479.2:p.Tyr432Phe
ENST00000245479.2:c.1295A>T ENSP00000245479.2:p.Tyr432Phe
NM_000346.3:c.1295A>T NP_000337.1:p.Tyr432Phe
NM_000346.4:c.1295A>T MANE Select NP_000337.1:p.Tyr432Phe
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