Canonical Allele Identifier: CA293782164
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs991888087
MyVariant Identifiers: chr17:g.70118887C>T (hg19) chr17:g.72122746C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122746C>T , CM000679.2:g.72122746C>T GRCh38
NC_000017.10:g.70118887C>T , CM000679.1:g.70118887C>T GRCh37
NC_000017.9:g.67630482C>T NCBI36
NG_012490.1:g.6727C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.459C>T MANE Select ENSP00000245479.2:p.Pro153=
ENST00000245479.2:c.459C>T ENSP00000245479.2:p.Pro153=
NM_000346.3:c.459C>T NP_000337.1:p.Pro153=
NM_000346.4:c.459C>T MANE Select NP_000337.1:p.Pro153=
Search 100 bp 5'
Search 100 bp 3'