Canonical Allele Identifier: CA400866512
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs368864961
MyVariant Identifiers: chr17:g.70118965G>T (hg19) chr17:g.72122824G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122824G>T , CM000679.2:g.72122824G>T GRCh38
NC_000017.10:g.70118965G>T , CM000679.1:g.70118965G>T GRCh37
NC_000017.9:g.67630560G>T NCBI36
NG_012490.1:g.6805G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.537G>T MANE Select ENSP00000245479.2:p.Arg179Ser
ENST00000245479.2:c.537G>T ENSP00000245479.2:p.Arg179Ser
NM_000346.3:c.537G>T NP_000337.1:p.Arg179Ser
NM_000346.4:c.537G>T MANE Select NP_000337.1:p.Arg179Ser
Search 100 bp 5'
Search 100 bp 3'