Canonical Allele Identifier: CA501352036
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1227778430
MyVariant Identifiers: chr17:g.70119778A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123637A>G , CM000679.2:g.72123637A>G GRCh38
NC_000017.10:g.70119778A>G , CM000679.1:g.70119778A>G GRCh37
NC_000017.9:g.67631373A>G NCBI36
NG_012490.1:g.7618A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.780A>G MANE Select ENSP00000245479.2:p.Pro260=
ENST00000245479.2:c.780A>G ENSP00000245479.2:p.Pro260=
NM_000346.3:c.780A>G NP_000337.1:p.Pro260=
NM_000346.4:c.780A>G MANE Select NP_000337.1:p.Pro260=
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