Canonical Allele Identifier: CA2129502471
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663161A= , CM000676.2:g.36663161A= GRCh38
NC_000014.8:g.37132366A= , CM000676.1:g.37132366A= GRCh37
NC_000014.7:g.36202117A= NCBI36
NG_013357.1:g.10594A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.269A= MANE Select ENSP00000355245.6:p.Tyr90=
ENST00000361487.6:c.269A= ENSP00000355245.6:p.Tyr90=
ENST00000402703.6:c.269A= ENSP00000384817.2:p.Tyr90=
ENST00000554201.1:c.-293A= ENSP00000450434.1:n.-293A=
NM_006194.3:c.269A= NP_006185.1:p.Tyr90=
NM_001372076.1:c.269A= MANE Select NP_001359005.1:p.Tyr90=
NM_006194.4:c.269A= NP_006185.1:p.Tyr90=