Canonical Allele Identifier: CA2734002342
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143249796

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123505T>G , CM000679.2:g.72123505T>G GRCh38
NC_000017.10:g.70119646T>G , CM000679.1:g.70119646T>G GRCh37
NC_000017.9:g.67631241T>G NCBI36
NG_012490.1:g.7486T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.686-38T>G MANE Select ENSP00000245479.2:n.686-38T>G
ENST00000245479.2:c.686-38T>G ENSP00000245479.2:n.686-38T>G
NM_000346.3:c.686-38T>G NP_000337.1:n.686-38T>G
NM_000346.4:c.686-38T>G MANE Select NP_000337.1:n.686-38T>G