Canonical Allele Identifier: CA2733951208
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1255195470

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123496C>A , CM000679.2:g.72123496C>A GRCh38
NC_000017.10:g.70119637C>A , CM000679.1:g.70119637C>A GRCh37
NC_000017.9:g.67631232C>A NCBI36
NG_012490.1:g.7477C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.686-47C>A MANE Select ENSP00000245479.2:n.686-47C>A
ENST00000245479.2:c.686-47C>A ENSP00000245479.2:n.686-47C>A
NM_000346.3:c.686-47C>A NP_000337.1:n.686-47C>A
NM_000346.4:c.686-47C>A MANE Select NP_000337.1:n.686-47C>A