Canonical Allele Identifier: CA2810344926
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122458T>G , CM000679.2:g.72122458T>G GRCh38
NC_000017.10:g.70118599T>G , CM000679.1:g.70118599T>G GRCh37
NC_000017.9:g.67630194T>G NCBI36
NG_012490.1:g.6439T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-261T>G MANE Select ENSP00000245479.2:n.432-261T>G
ENST00000245479.2:c.432-261T>G ENSP00000245479.2:n.432-261T>G
NM_000346.3:c.432-261T>G NP_000337.1:n.432-261T>G
NM_000346.4:c.432-261T>G MANE Select NP_000337.1:n.432-261T>G