Canonical Allele Identifier: CA2810344897
Gene: SOX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122324G>C , CM000679.2:g.72122324G>C GRCh38
NC_000017.10:g.70118465G>C , CM000679.1:g.70118465G>C GRCh37
NC_000017.9:g.67630060G>C NCBI36
NG_012490.1:g.6305G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-395G>C MANE Select ENSP00000245479.2:n.432-395G>C
ENST00000245479.2:c.432-395G>C ENSP00000245479.2:n.432-395G>C
NM_000346.3:c.432-395G>C NP_000337.1:n.432-395G>C
NM_000346.4:c.432-395G>C MANE Select NP_000337.1:n.432-395G>C