Canonical Allele Identifier: CA2129502195
Gene: PAX9 HGNC NCBI

Linked Data

dbSNP Id: rs1881335592
gnomAD v4: 14-36662880-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36662880G>C , CM000676.2:g.36662880G>C GRCh38
NC_000014.8:g.37132085G>C , CM000676.1:g.37132085G>C GRCh37
NC_000014.7:g.36201836G>C NCBI36
NG_013357.1:g.10313G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.5-17G>C MANE Select ENSP00000355245.6:n.5-17G>C
ENST00000555639.2:c.5-17G>C ENSP00000501203.1:n.5-17G>C
ENST00000361487.6:c.5-17G>C ENSP00000355245.6:n.5-17G>C
ENST00000402703.6:c.5-17G>C ENSP00000384817.2:n.5-17G>C
ENST00000554201.1:c.-574G>C ENSP00000450434.1:n.-574G>C
ENST00000555639.1:n.307-17G>C
NM_006194.3:c.5-17G>C NP_006185.1:n.5-17G>C
NM_001372076.1:c.5-17G>C MANE Select NP_001359005.1:n.5-17G>C
NM_006194.4:c.5-17G>C NP_006185.1:n.5-17G>C
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