Canonical Allele Identifier: CA2129502468
Gene: PAX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663158C= , CM000676.2:g.36663158C= GRCh38
NC_000014.8:g.37132363C= , CM000676.1:g.37132363C= GRCh37
NC_000014.7:g.36202114C= NCBI36
NG_013357.1:g.10591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.266C= MANE Select ENSP00000355245.6:p.Thr89=
ENST00000361487.6:c.266C= ENSP00000355245.6:p.Thr89=
ENST00000402703.6:c.266C= ENSP00000384817.2:p.Thr89=
ENST00000554201.1:c.-296C= ENSP00000450434.1:n.-296C=
NM_006194.3:c.266C= NP_006185.1:p.Thr89=
NM_001372076.1:c.266C= MANE Select NP_001359005.1:p.Thr89=
NM_006194.4:c.266C= NP_006185.1:p.Thr89=
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