Canonical Allele Identifier: CA962020355
Gene: PAX9 HGNC NCBI

Linked Data

dbSNP Id: rs768757265
gnomAD v3: 14-36662878-C-A
gnomAD v4: 14-36662878-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36662878C>A , CM000676.2:g.36662878C>A GRCh38
NC_000014.8:g.37132083C>A , CM000676.1:g.37132083C>A GRCh37
NC_000014.7:g.36201834C>A NCBI36
NG_013357.1:g.10311C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.5-19C>A MANE Select ENSP00000355245.6:n.5-19C>A
ENST00000555639.2:c.5-19C>A ENSP00000501203.1:n.5-19C>A
ENST00000361487.6:c.5-19C>A ENSP00000355245.6:n.5-19C>A
ENST00000402703.6:c.5-19C>A ENSP00000384817.2:n.5-19C>A
ENST00000554201.1:c.-576C>A ENSP00000450434.1:n.-576C>A
ENST00000555639.1:n.307-19C>A
NM_006194.3:c.5-19C>A NP_006185.1:n.5-19C>A
NM_001372076.1:c.5-19C>A MANE Select NP_001359005.1:n.5-19C>A
NM_006194.4:c.5-19C>A NP_006185.1:n.5-19C>A
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