Canonical Allele Identifier: CA2129503009
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663480C= , CM000676.2:g.36663480C= GRCh38
NC_000014.8:g.37132685C= , CM000676.1:g.37132685C= GRCh37
NC_000014.7:g.36202436C= NCBI36
NG_013357.1:g.10913C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.588C= MANE Select ENSP00000355245.6:p.His196=
ENST00000361487.6:c.588C= ENSP00000355245.6:p.His196=
ENST00000402703.6:c.588C= ENSP00000384817.2:p.His196=
ENST00000554201.1:c.27C= ENSP00000450434.1:p.His9=
NM_006194.3:c.588C= NP_006185.1:p.His196=
NM_001372076.1:c.588C= MANE Select NP_001359005.1:p.His196=
NM_006194.4:c.588C= NP_006185.1:p.His196=