Canonical Allele Identifier: CA2273926319
Gene: SOX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123528T= , CM000679.2:g.72123528T= GRCh38
NC_000017.10:g.70119669T= , CM000679.1:g.70119669T= GRCh37
NC_000017.9:g.67631264T= NCBI36
NG_012490.1:g.7509T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.686-15T= MANE Select ENSP00000245479.2:n.686-15T=
ENST00000245479.2:c.686-15T= ENSP00000245479.2:n.686-15T=
NM_000346.3:c.686-15T= NP_000337.1:n.686-15T=
NM_000346.4:c.686-15T= MANE Select NP_000337.1:n.686-15T=
Search 100 bp 5'
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