Canonical Allele Identifier: CA389466522
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132389T>A (hg19) chr14:g.36663184T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663184T>A , CM000676.2:g.36663184T>A GRCh38
NC_000014.8:g.37132389T>A , CM000676.1:g.37132389T>A GRCh37
NC_000014.7:g.36202140T>A NCBI36
NG_013357.1:g.10617T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.292T>A MANE Select ENSP00000355245.6:p.Phe98Ile
ENST00000361487.6:c.292T>A ENSP00000355245.6:p.Phe98Ile
ENST00000402703.6:c.292T>A ENSP00000384817.2:p.Phe98Ile
ENST00000554201.1:c.-270T>A ENSP00000450434.1:n.-270T>A
NM_006194.3:c.292T>A NP_006185.1:p.Phe98Ile
NM_001372076.1:c.292T>A MANE Select NP_001359005.1:p.Phe98Ile
NM_006194.4:c.292T>A NP_006185.1:p.Phe98Ile
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