Canonical Allele Identifier: CA389467131
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132683C>A (hg19) chr14:g.36663478C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663478C>A , CM000676.2:g.36663478C>A GRCh38
NC_000014.8:g.37132683C>A , CM000676.1:g.37132683C>A GRCh37
NC_000014.7:g.36202434C>A NCBI36
NG_013357.1:g.10911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.586C>A MANE Select ENSP00000355245.6:p.His196Asn
ENST00000361487.6:c.586C>A ENSP00000355245.6:p.His196Asn
ENST00000402703.6:c.586C>A ENSP00000384817.2:p.His196Asn
ENST00000554201.1:c.25C>A ENSP00000450434.1:p.His9Asn
NM_006194.3:c.586C>A NP_006185.1:p.His196Asn
NM_001372076.1:c.586C>A MANE Select NP_001359005.1:p.His196Asn
NM_006194.4:c.586C>A NP_006185.1:p.His196Asn
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