Canonical Allele Identifier: CA389466638
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663238A>G , CM000676.2:g.36663238A>G GRCh38
NC_000014.8:g.37132443A>G , CM000676.1:g.37132443A>G GRCh37
NC_000014.7:g.36202194A>G NCBI36
NG_013357.1:g.10671A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.346A>G MANE Select ENSP00000355245.6:p.Asn116Asp
ENST00000361487.6:c.346A>G ENSP00000355245.6:p.Asn116Asp
ENST00000402703.6:c.346A>G ENSP00000384817.2:p.Asn116Asp
ENST00000554201.1:c.-216A>G ENSP00000450434.1:n.-216A>G
NM_006194.3:c.346A>G NP_006185.1:p.Asn116Asp
NM_001372076.1:c.346A>G MANE Select NP_001359005.1:p.Asn116Asp
NM_006194.4:c.346A>G NP_006185.1:p.Asn116Asp