Canonical Allele Identifier: CA2129502518
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663199C= , CM000676.2:g.36663199C= GRCh38
NC_000014.8:g.37132404C= , CM000676.1:g.37132404C= GRCh37
NC_000014.7:g.36202155C= NCBI36
NG_013357.1:g.10632C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.307C= MANE Select ENSP00000355245.6:p.Arg103=
ENST00000361487.6:c.307C= ENSP00000355245.6:p.Arg103=
ENST00000402703.6:c.307C= ENSP00000384817.2:p.Arg103=
ENST00000554201.1:c.-255C= ENSP00000450434.1:n.-255C=
NM_006194.3:c.307C= NP_006185.1:p.Arg103=
NM_001372076.1:c.307C= MANE Select NP_001359005.1:p.Arg103=
NM_006194.4:c.307C= NP_006185.1:p.Arg103=