Canonical Allele Identifier: CA774799530
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1202093634
gnomAD v3: 17-72122475-G-A
gnomAD v4: 17-72122475-G-A
MyVariant Identifiers: chr17:g.70118616G>A (hg19) chr17:g.72122475G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122475G>A , CM000679.2:g.72122475G>A GRCh38
NC_000017.10:g.70118616G>A , CM000679.1:g.70118616G>A GRCh37
NC_000017.9:g.67630211G>A NCBI36
NG_012490.1:g.6456G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-244G>A MANE Select ENSP00000245479.2:n.432-244G>A
ENST00000245479.2:c.432-244G>A ENSP00000245479.2:n.432-244G>A
NM_000346.3:c.432-244G>A NP_000337.1:n.432-244G>A
NM_000346.4:c.432-244G>A MANE Select NP_000337.1:n.432-244G>A
Search 100 bp 5'
Search 100 bp 3'