Canonical Allele Identifier: CA501432687
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1482252629
gnomAD v2: 17-70120021-G-A
gnomAD v4: 17-72123880-G-A
COSMIC: COSM5825230
MyVariant Identifiers: chr17:g.70120021G>A (hg19) chr17:g.72123880G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123880G>A , CM000679.2:g.72123880G>A GRCh38
NC_000017.10:g.70120021G>A , CM000679.1:g.70120021G>A GRCh37
NC_000017.9:g.67631616G>A NCBI36
NG_012490.1:g.7861G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.1023G>A MANE Select ENSP00000245479.2:p.Ala341=
ENST00000245479.2:c.1023G>A ENSP00000245479.2:p.Ala341=
NM_000346.3:c.1023G>A NP_000337.1:p.Ala341=
NM_000346.4:c.1023G>A MANE Select NP_000337.1:p.Ala341=
Search 100 bp 5'
Search 100 bp 3'