Canonical Allele Identifier: CA2129502473
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663162C= , CM000676.2:g.36663162C= GRCh38
NC_000014.8:g.37132367C= , CM000676.1:g.37132367C= GRCh37
NC_000014.7:g.36202118C= NCBI36
NG_013357.1:g.10595C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.270C= MANE Select ENSP00000355245.6:p.Tyr90=
ENST00000361487.6:c.270C= ENSP00000355245.6:p.Tyr90=
ENST00000402703.6:c.270C= ENSP00000384817.2:p.Tyr90=
ENST00000554201.1:c.-292C= ENSP00000450434.1:n.-292C=
NM_006194.3:c.270C= NP_006185.1:p.Tyr90=
NM_001372076.1:c.270C= MANE Select NP_001359005.1:p.Tyr90=
NM_006194.4:c.270C= NP_006185.1:p.Tyr90=