Canonical Allele Identifier: CA2273925750
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122496G= , CM000679.2:g.72122496G= GRCh38
NC_000017.10:g.70118637G= , CM000679.1:g.70118637G= GRCh37
NC_000017.9:g.67630232G= NCBI36
NG_012490.1:g.6477G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-223G= MANE Select ENSP00000245479.2:n.432-223G=
ENST00000245479.2:c.432-223G= ENSP00000245479.2:n.432-223G=
NM_000346.3:c.432-223G= NP_000337.1:n.432-223G=
NM_000346.4:c.432-223G= MANE Select NP_000337.1:n.432-223G=