Canonical Allele Identifier: CA389466435
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132350A>G (hg19) chr14:g.36663145A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663145A>G , CM000676.2:g.36663145A>G GRCh38
NC_000014.8:g.37132350A>G , CM000676.1:g.37132350A>G GRCh37
NC_000014.7:g.36202101A>G NCBI36
NG_013357.1:g.10578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.253A>G MANE Select ENSP00000355245.6:p.Lys85Glu
ENST00000361487.6:c.253A>G ENSP00000355245.6:p.Lys85Glu
ENST00000402703.6:c.253A>G ENSP00000384817.2:p.Lys85Glu
ENST00000554201.1:c.-309A>G ENSP00000450434.1:n.-309A>G
NM_006194.3:c.253A>G NP_006185.1:p.Lys85Glu
NM_001372076.1:c.253A>G MANE Select NP_001359005.1:p.Lys85Glu
NM_006194.4:c.253A>G NP_006185.1:p.Lys85Glu
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