Canonical Allele Identifier: CA2273926356
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123596C= , CM000679.2:g.72123596C= GRCh38
NC_000017.10:g.70119737C= , CM000679.1:g.70119737C= GRCh37
NC_000017.9:g.67631332C= NCBI36
NG_012490.1:g.7577C=

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.739C= MANE Select ENSP00000245479.2:p.Pro247=
ENST00000245479.2:c.739C= ENSP00000245479.2:p.Pro247=
NM_000346.3:c.739C= NP_000337.1:p.Pro247=
NM_000346.4:c.739C= MANE Select NP_000337.1:p.Pro247=