Canonical Allele Identifier: CA389466554
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132401A>T (hg19) chr14:g.36663196A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663196A>T , CM000676.2:g.36663196A>T GRCh38
NC_000014.8:g.37132401A>T , CM000676.1:g.37132401A>T GRCh37
NC_000014.7:g.36202152A>T NCBI36
NG_013357.1:g.10629A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.304A>T MANE Select ENSP00000355245.6:p.Ile102Phe
ENST00000361487.6:c.304A>T ENSP00000355245.6:p.Ile102Phe
ENST00000402703.6:c.304A>T ENSP00000384817.2:p.Ile102Phe
ENST00000554201.1:c.-258A>T ENSP00000450434.1:n.-258A>T
NM_006194.3:c.304A>T NP_006185.1:p.Ile102Phe
NM_001372076.1:c.304A>T MANE Select NP_001359005.1:p.Ile102Phe
NM_006194.4:c.304A>T NP_006185.1:p.Ile102Phe
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