Canonical Allele Identifier: CA7158900
Gene: PAX9 HGNC NCBI

Linked Data

dbSNP Id: rs751740330

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36662884G>A , CM000676.2:g.36662884G>A GRCh38
NC_000014.8:g.37132089G>A , CM000676.1:g.37132089G>A GRCh37
NC_000014.7:g.36201840G>A NCBI36
NG_013357.1:g.10317G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.5-13G>A MANE Select ENSP00000355245.6:n.5-13G>A
ENST00000555639.2:c.5-13G>A ENSP00000501203.1:n.5-13G>A
ENST00000361487.6:c.5-13G>A ENSP00000355245.6:n.5-13G>A
ENST00000402703.6:c.5-13G>A ENSP00000384817.2:n.5-13G>A
ENST00000554201.1:c.-570G>A ENSP00000450434.1:n.-570G>A
ENST00000555639.1:n.307-13G>A
NM_006194.3:c.5-13G>A NP_006185.1:n.5-13G>A
NM_001372076.1:c.5-13G>A MANE Select NP_001359005.1:n.5-13G>A
NM_006194.4:c.5-13G>A NP_006185.1:n.5-13G>A