Canonical Allele Identifier: CA2129503267
Gene: PAX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663641T= , CM000676.2:g.36663641T= GRCh38
NC_000014.8:g.37132846T= , CM000676.1:g.37132846T= GRCh37
NC_000014.7:g.36202597T= NCBI36
NG_013357.1:g.11074T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.631+118T= MANE Select ENSP00000355245.6:n.631+118T=
ENST00000361487.6:c.631+118T= ENSP00000355245.6:n.631+118T=
ENST00000402703.6:c.631+118T= ENSP00000384817.2:n.631+118T=
ENST00000554201.1:c.70+118T= ENSP00000450434.1:n.70+118T=
NM_006194.3:c.631+118T= NP_006185.1:n.631+118T=
NM_001372076.1:c.631+118T= MANE Select NP_001359005.1:n.631+118T=
NM_006194.4:c.631+118T= NP_006185.1:n.631+118T=
Search 100 bp 5'
Search 100 bp 3'