Canonical Allele Identifier: CA389466132
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132207T>A (hg19) chr14:g.36663002T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663002T>A , CM000676.2:g.36663002T>A GRCh38
NC_000014.8:g.37132207T>A , CM000676.1:g.37132207T>A GRCh37
NC_000014.7:g.36201958T>A NCBI36
NG_013357.1:g.10435T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.110T>A MANE Select ENSP00000355245.6:p.Ile37Asn
ENST00000555639.2:c.110T>A ENSP00000501203.1:p.Ile37Asn
ENST00000361487.6:c.110T>A ENSP00000355245.6:p.Ile37Asn
ENST00000402703.6:c.110T>A ENSP00000384817.2:p.Ile37Asn
ENST00000554201.1:c.-452T>A ENSP00000450434.1:n.-452T>A
ENST00000555639.1:n.412T>A
NM_006194.3:c.110T>A NP_006185.1:p.Ile37Asn
NM_001372076.1:c.110T>A MANE Select NP_001359005.1:p.Ile37Asn
NM_006194.4:c.110T>A NP_006185.1:p.Ile37Asn
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