Canonical Allele Identifier: CA627589955
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1255195470

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123496C>T , CM000679.2:g.72123496C>T GRCh38
NC_000017.10:g.70119637C>T , CM000679.1:g.70119637C>T GRCh37
NC_000017.9:g.67631232C>T NCBI36
NG_012490.1:g.7477C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.686-47C>T MANE Select ENSP00000245479.2:n.686-47C>T
ENST00000245479.2:c.686-47C>T ENSP00000245479.2:n.686-47C>T
NM_000346.3:c.686-47C>T NP_000337.1:n.686-47C>T
NM_000346.4:c.686-47C>T MANE Select NP_000337.1:n.686-47C>T