Canonical Allele Identifier: CA2624603646
Gene: PAX9 HGNC NCBI

Linked Data

gnomAD v4: 14-36663587-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663587C>T , CM000676.2:g.36663587C>T GRCh38
NC_000014.8:g.37132792C>T , CM000676.1:g.37132792C>T GRCh37
NC_000014.7:g.36202543C>T NCBI36
NG_013357.1:g.11020C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.631+64C>T MANE Select ENSP00000355245.6:n.631+64C>T
ENST00000361487.6:c.631+64C>T ENSP00000355245.6:n.631+64C>T
ENST00000402703.6:c.631+64C>T ENSP00000384817.2:n.631+64C>T
ENST00000554201.1:c.70+64C>T ENSP00000450434.1:n.70+64C>T
NM_006194.3:c.631+64C>T NP_006185.1:n.631+64C>T
NM_001372076.1:c.631+64C>T MANE Select NP_001359005.1:n.631+64C>T
NM_006194.4:c.631+64C>T NP_006185.1:n.631+64C>T
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