Canonical Allele Identifier: CA2273926236
Gene: SOX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123407G= , CM000679.2:g.72123407G= GRCh38
NC_000017.10:g.70119548G= , CM000679.1:g.70119548G= GRCh37
NC_000017.9:g.67631143G= NCBI36
NG_012490.1:g.7388G=

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.686-136G= MANE Select ENSP00000245479.2:n.686-136G=
ENST00000245479.2:c.686-136G= ENSP00000245479.2:n.686-136G=
NM_000346.3:c.686-136G= NP_000337.1:n.686-136G=
NM_000346.4:c.686-136G= MANE Select NP_000337.1:n.686-136G=
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