Canonical Allele Identifier: CA2273925746
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1908129502

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122496del , CM000679.2:g.72122496del GRCh38
NC_000017.10:g.70118637del , CM000679.1:g.70118637del GRCh37
NC_000017.9:g.67630232del NCBI36
NG_012490.1:g.6477del

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-223del MANE Select ENSP00000245479.2:n.432-223del
ENST00000245479.2:c.432-223del ENSP00000245479.2:n.432-223del
NM_000346.3:c.432-223del NP_000337.1:n.432-223del
NM_000346.4:c.432-223del MANE Select NP_000337.1:n.432-223del