Canonical Allele Identifier: CA2129502847
Gene: PAX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663398C= , CM000676.2:g.36663398C= GRCh38
NC_000014.8:g.37132603C= , CM000676.1:g.37132603C= GRCh37
NC_000014.7:g.36202354C= NCBI36
NG_013357.1:g.10831C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.506C= MANE Select ENSP00000355245.6:p.Ala169=
ENST00000361487.6:c.506C= ENSP00000355245.6:p.Ala169=
ENST00000402703.6:c.506C= ENSP00000384817.2:p.Ala169=
ENST00000554201.1:c.-56C= ENSP00000450434.1:n.-56C=
NM_006194.3:c.506C= NP_006185.1:p.Ala169=
NM_001372076.1:c.506C= MANE Select NP_001359005.1:p.Ala169=
NM_006194.4:c.506C= NP_006185.1:p.Ala169=
Search 100 bp 5'
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