Canonical Allele Identifier: CA2576374478
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143244813
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122705C>T , CM000679.2:g.72122705C>T GRCh38
NC_000017.10:g.70118846C>T , CM000679.1:g.70118846C>T GRCh37
NC_000017.9:g.67630441C>T NCBI36
NG_012490.1:g.6686C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.432-14C>T MANE Select ENSP00000245479.2:n.432-14C>T
ENST00000245479.2:c.432-14C>T ENSP00000245479.2:n.432-14C>T
NM_000346.3:c.432-14C>T NP_000337.1:n.432-14C>T
NM_000346.4:c.432-14C>T MANE Select NP_000337.1:n.432-14C>T
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