Canonical Allele Identifier: CA400866511
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs368864961

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122824G>C , CM000679.2:g.72122824G>C GRCh38
NC_000017.10:g.70118965G>C , CM000679.1:g.70118965G>C GRCh37
NC_000017.9:g.67630560G>C NCBI36
NG_012490.1:g.6805G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.537G>C MANE Select ENSP00000245479.2:p.Arg179Ser
ENST00000245479.2:c.537G>C ENSP00000245479.2:p.Arg179Ser
NM_000346.3:c.537G>C NP_000337.1:p.Arg179Ser
NM_000346.4:c.537G>C MANE Select NP_000337.1:p.Arg179Ser