Canonical Allele Identifier: CA2129502797
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663370T= , CM000676.2:g.36663370T= GRCh38
NC_000014.8:g.37132575T= , CM000676.1:g.37132575T= GRCh37
NC_000014.7:g.36202326T= NCBI36
NG_013357.1:g.10803T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.478T= MANE Select ENSP00000355245.6:p.Tyr160=
ENST00000361487.6:c.478T= ENSP00000355245.6:p.Tyr160=
ENST00000402703.6:c.478T= ENSP00000384817.2:p.Tyr160=
ENST00000554201.1:c.-84T= ENSP00000450434.1:n.-84T=
NM_006194.3:c.478T= NP_006185.1:p.Tyr160=
NM_001372076.1:c.478T= MANE Select NP_001359005.1:p.Tyr160=
NM_006194.4:c.478T= NP_006185.1:p.Tyr160=