Canonical Allele Identifier: CA2734002600
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143249905
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123525T>A , CM000679.2:g.72123525T>A GRCh38
NC_000017.10:g.70119666T>A , CM000679.1:g.70119666T>A GRCh37
NC_000017.9:g.67631261T>A NCBI36
NG_012490.1:g.7506T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.686-18T>A MANE Select ENSP00000245479.2:n.686-18T>A
ENST00000245479.2:c.686-18T>A ENSP00000245479.2:n.686-18T>A
NM_000346.3:c.686-18T>A NP_000337.1:n.686-18T>A
NM_000346.4:c.686-18T>A MANE Select NP_000337.1:n.686-18T>A
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