Canonical Allele Identifier: CA389466485
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132372A>T (hg19) chr14:g.36663167A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663167A>T , CM000676.2:g.36663167A>T GRCh38
NC_000014.8:g.37132372A>T , CM000676.1:g.37132372A>T GRCh37
NC_000014.7:g.36202123A>T NCBI36
NG_013357.1:g.10600A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.275A>T MANE Select ENSP00000355245.6:p.Gln92Leu
ENST00000361487.6:c.275A>T ENSP00000355245.6:p.Gln92Leu
ENST00000402703.6:c.275A>T ENSP00000384817.2:p.Gln92Leu
ENST00000554201.1:c.-287A>T ENSP00000450434.1:n.-287A>T
NM_006194.3:c.275A>T NP_006185.1:p.Gln92Leu
NM_001372076.1:c.275A>T MANE Select NP_001359005.1:p.Gln92Leu
NM_006194.4:c.275A>T NP_006185.1:p.Gln92Leu
Search 100 bp 5'
Search 100 bp 3'