Canonical Allele Identifier: CA389466341
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132303G>T (hg19) chr14:g.36663098G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663098G>T , CM000676.2:g.36663098G>T GRCh38
NC_000014.8:g.37132303G>T , CM000676.1:g.37132303G>T GRCh37
NC_000014.7:g.36202054G>T NCBI36
NG_013357.1:g.10531G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.206G>T MANE Select ENSP00000355245.6:p.Gly69Val
ENST00000555639.2:c.206G>T ENSP00000501203.1:p.Gly69Val
ENST00000361487.6:c.206G>T ENSP00000355245.6:p.Gly69Val
ENST00000402703.6:c.206G>T ENSP00000384817.2:p.Gly69Val
ENST00000554201.1:c.-356G>T ENSP00000450434.1:n.-356G>T
ENST00000555639.1:n.508G>T
NM_006194.3:c.206G>T NP_006185.1:p.Gly69Val
NM_001372076.1:c.206G>T MANE Select NP_001359005.1:p.Gly69Val
NM_006194.4:c.206G>T NP_006185.1:p.Gly69Val
Search 100 bp 5'
Search 100 bp 3'