Canonical Allele Identifier: CA2273925652
Gene: SOX9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122325T= , CM000679.2:g.72122325T= GRCh38
NC_000017.10:g.70118466T= , CM000679.1:g.70118466T= GRCh37
NC_000017.9:g.67630061T= NCBI36
NG_012490.1:g.6306T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-394T= MANE Select ENSP00000245479.2:n.432-394T=
ENST00000245479.2:c.432-394T= ENSP00000245479.2:n.432-394T=
NM_000346.3:c.432-394T= NP_000337.1:n.432-394T=
NM_000346.4:c.432-394T= MANE Select NP_000337.1:n.432-394T=
Search 100 bp 5'
Search 100 bp 3'