Canonical Allele Identifier: CA2273925692
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122390T= , CM000679.2:g.72122390T= GRCh38
NC_000017.10:g.70118531T= , CM000679.1:g.70118531T= GRCh37
NC_000017.9:g.67630126T= NCBI36
NG_012490.1:g.6371T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-329T= MANE Select ENSP00000245479.2:n.432-329T=
ENST00000245479.2:c.432-329T= ENSP00000245479.2:n.432-329T=
NM_000346.3:c.432-329T= NP_000337.1:n.432-329T=
NM_000346.4:c.432-329T= MANE Select NP_000337.1:n.432-329T=