Canonical Allele Identifier: CA389466551
Gene: PAX9 HGNC NCBI

Linked Data

gnomAD v4: 14-36663195-G-T
MyVariant Identifiers: chr14:g.37132400G>T (hg19) chr14:g.36663195G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663195G>T , CM000676.2:g.36663195G>T GRCh38
NC_000014.8:g.37132400G>T , CM000676.1:g.37132400G>T GRCh37
NC_000014.7:g.36202151G>T NCBI36
NG_013357.1:g.10628G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.303G>T MANE Select ENSP00000355245.6:p.Glu101Asp
ENST00000361487.6:c.303G>T ENSP00000355245.6:p.Glu101Asp
ENST00000402703.6:c.303G>T ENSP00000384817.2:p.Glu101Asp
ENST00000554201.1:c.-259G>T ENSP00000450434.1:n.-259G>T
NM_006194.3:c.303G>T NP_006185.1:p.Glu101Asp
NM_001372076.1:c.303G>T MANE Select NP_001359005.1:p.Glu101Asp
NM_006194.4:c.303G>T NP_006185.1:p.Glu101Asp
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