Canonical Allele Identifier: CA501351992
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1175244556
gnomAD v2: 17-70119727-C-T
gnomAD v4: 17-72123586-C-T
MyVariant Identifiers: chr17:g.70119727C>T (hg19) chr17:g.72123586C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123586C>T , CM000679.2:g.72123586C>T GRCh38
NC_000017.10:g.70119727C>T , CM000679.1:g.70119727C>T GRCh37
NC_000017.9:g.67631322C>T NCBI36
NG_012490.1:g.7567C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.729C>T MANE Select ENSP00000245479.2:p.Thr243=
ENST00000245479.2:c.729C>T ENSP00000245479.2:p.Thr243=
NM_000346.3:c.729C>T NP_000337.1:p.Thr243=
NM_000346.4:c.729C>T MANE Select NP_000337.1:p.Thr243=
Search 100 bp 5'
Search 100 bp 3'