Canonical Allele Identifier: CA774799528
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1443409940
MyVariant Identifiers: chr17:g.70118590T>C (hg19) chr17:g.72122449T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122449T>C , CM000679.2:g.72122449T>C GRCh38
NC_000017.10:g.70118590T>C , CM000679.1:g.70118590T>C GRCh37
NC_000017.9:g.67630185T>C NCBI36
NG_012490.1:g.6430T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-270T>C MANE Select ENSP00000245479.2:n.432-270T>C
ENST00000245479.2:c.432-270T>C ENSP00000245479.2:n.432-270T>C
NM_000346.3:c.432-270T>C NP_000337.1:n.432-270T>C
NM_000346.4:c.432-270T>C MANE Select NP_000337.1:n.432-270T>C
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