Canonical Allele Identifier: CA501432865
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143255173
MyVariant Identifiers: chr17:g.70120180A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72124039A>C , CM000679.2:g.72124039A>C GRCh38
NC_000017.10:g.70120180A>C , CM000679.1:g.70120180A>C GRCh37
NC_000017.9:g.67631775A>C NCBI36
NG_012490.1:g.8020A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.1182A>C MANE Select ENSP00000245479.2:p.Arg394=
ENST00000245479.2:c.1182A>C ENSP00000245479.2:p.Arg394=
NM_000346.3:c.1182A>C NP_000337.1:p.Arg394=
NM_000346.4:c.1182A>C MANE Select NP_000337.1:p.Arg394=
Search 100 bp 5'
Search 100 bp 3'