Canonical Allele Identifier: CA486097661
Gene: PAX9 HGNC NCBI

Linked Data

dbSNP Id: rs1191578972
gnomAD v2: 14-37132400-G-A
gnomAD v3: 14-36663195-G-A
gnomAD v4: 14-36663195-G-A
MyVariant Identifiers: chr14:g.37132400G>A (hg19) chr14:g.36663195G>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.303G>A MANE Select ENSP00000355245.6:p.Glu101=
ENST00000361487.6:c.303G>A ENSP00000355245.6:p.Glu101=
ENST00000402703.6:c.303G>A ENSP00000384817.2:p.Glu101=
ENST00000554201.1:c.-259G>A ENSP00000450434.1:n.-259G>A
NM_006194.3:c.303G>A NP_006185.1:p.Glu101=
NM_001372076.1:c.303G>A MANE Select NP_001359005.1:p.Glu101=
NM_006194.4:c.303G>A NP_006185.1:p.Glu101=
Search 100 bp 5'
Search 100 bp 3'