Canonical Allele Identifier: CA2129503001
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663476C= , CM000676.2:g.36663476C= GRCh38
NC_000014.8:g.37132681C= , CM000676.1:g.37132681C= GRCh37
NC_000014.7:g.36202432C= NCBI36
NG_013357.1:g.10909C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.584C= MANE Select ENSP00000355245.6:p.Ser195=
ENST00000361487.6:c.584C= ENSP00000355245.6:p.Ser195=
ENST00000402703.6:c.584C= ENSP00000384817.2:p.Ser195=
ENST00000554201.1:c.23C= ENSP00000450434.1:p.Ser8=
NM_006194.3:c.584C= NP_006185.1:p.Ser195=
NM_001372076.1:c.584C= MANE Select NP_001359005.1:p.Ser195=
NM_006194.4:c.584C= NP_006185.1:p.Ser195=