Canonical Allele Identifier: CA2273925673
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122366A= , CM000679.2:g.72122366A= GRCh38
NC_000017.10:g.70118507A= , CM000679.1:g.70118507A= GRCh37
NC_000017.9:g.67630102A= NCBI36
NG_012490.1:g.6347A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-353A= MANE Select ENSP00000245479.2:n.432-353A=
ENST00000245479.2:c.432-353A= ENSP00000245479.2:n.432-353A=
NM_000346.3:c.432-353A= NP_000337.1:n.432-353A=
NM_000346.4:c.432-353A= MANE Select NP_000337.1:n.432-353A=