Canonical Allele Identifier: CA501351998
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143250573
MyVariant Identifiers: chr17:g.70119736G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123595G>A , CM000679.2:g.72123595G>A GRCh38
NC_000017.10:g.70119736G>A , CM000679.1:g.70119736G>A GRCh37
NC_000017.9:g.67631331G>A NCBI36
NG_012490.1:g.7576G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000245479.3:c.738G>A MANE Select ENSP00000245479.2:p.Gln246=
ENST00000245479.2:c.738G>A ENSP00000245479.2:p.Gln246=
NM_000346.3:c.738G>A NP_000337.1:p.Gln246=
NM_000346.4:c.738G>A MANE Select NP_000337.1:p.Gln246=