Canonical Allele Identifier: CA501432719
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2781525
ClinVar RCV Id: RCV003603250
dbSNP Id: rs1319508171
gnomAD v3: 17-72123925-G-A
gnomAD v4: 17-72123925-G-A
MyVariant Identifiers: chr17:g.70120066G>A (hg19) chr17:g.72123925G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123925G>A , CM000679.2:g.72123925G>A GRCh38
NC_000017.10:g.70120066G>A , CM000679.1:g.70120066G>A GRCh37
NC_000017.9:g.67631661G>A NCBI36
NG_012490.1:g.7906G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1068G>A MANE Select ENSP00000245479.2:p.Pro356=
ENST00000245479.2:c.1068G>A ENSP00000245479.2:p.Pro356=
NM_000346.3:c.1068G>A NP_000337.1:p.Pro356=
NM_000346.4:c.1068G>A MANE Select NP_000337.1:p.Pro356=
Search 100 bp 5'
Search 100 bp 3'