Canonical Allele Identifier: CA2273926428
Gene: SOX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123767C= , CM000679.2:g.72123767C= GRCh38
NC_000017.10:g.70119908C= , CM000679.1:g.70119908C= GRCh37
NC_000017.9:g.67631503C= NCBI36
NG_012490.1:g.7748C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.910C= MANE Select ENSP00000245479.2:p.Pro304=
ENST00000245479.2:c.910C= ENSP00000245479.2:p.Pro304=
NM_000346.3:c.910C= NP_000337.1:p.Pro304=
NM_000346.4:c.910C= MANE Select NP_000337.1:p.Pro304=
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