Canonical Allele Identifier: CA400866963
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1170758830

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123604G>T , CM000679.2:g.72123604G>T GRCh38
NC_000017.10:g.70119745G>T , CM000679.1:g.70119745G>T GRCh37
NC_000017.9:g.67631340G>T NCBI36
NG_012490.1:g.7585G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.747G>T MANE Select ENSP00000245479.2:p.Lys249Asn
ENST00000245479.2:c.747G>T ENSP00000245479.2:p.Lys249Asn
NM_000346.3:c.747G>T NP_000337.1:p.Lys249Asn
NM_000346.4:c.747G>T MANE Select NP_000337.1:p.Lys249Asn