Canonical Allele Identifier: CA774799505
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs1443691945
MyVariant Identifiers: chr17:g.70118520G>A (hg19) chr17:g.72122379G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72122379G>A , CM000679.2:g.72122379G>A GRCh38
NC_000017.10:g.70118520G>A , CM000679.1:g.70118520G>A GRCh37
NC_000017.9:g.67630115G>A NCBI36
NG_012490.1:g.6360G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.432-340G>A MANE Select ENSP00000245479.2:n.432-340G>A
ENST00000245479.2:c.432-340G>A ENSP00000245479.2:n.432-340G>A
NM_000346.3:c.432-340G>A NP_000337.1:n.432-340G>A
NM_000346.4:c.432-340G>A MANE Select NP_000337.1:n.432-340G>A
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