Canonical Allele Identifier: CA400868274
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143257158
MyVariant Identifiers: chr17:g.70120353A>T (hg19) chr17:g.72124212A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124212A>T , CM000679.2:g.72124212A>T GRCh38
NC_000017.10:g.70120353A>T , CM000679.1:g.70120353A>T GRCh37
NC_000017.9:g.67631948A>T NCBI36
NG_012490.1:g.8193A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1355A>T MANE Select ENSP00000245479.2:p.Tyr452Phe
ENST00000245479.2:c.1355A>T ENSP00000245479.2:p.Tyr452Phe
NM_000346.3:c.1355A>T NP_000337.1:p.Tyr452Phe
NM_000346.4:c.1355A>T MANE Select NP_000337.1:p.Tyr452Phe
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