Canonical Allele Identifier: CA389466085
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132185G>A (hg19) chr14:g.36662980G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36662980G>A , CM000676.2:g.36662980G>A GRCh38
NC_000014.8:g.37132185G>A , CM000676.1:g.37132185G>A GRCh37
NC_000014.7:g.36201936G>A NCBI36
NG_013357.1:g.10413G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.88G>A MANE Select ENSP00000355245.6:p.Val30Met
ENST00000555639.2:c.88G>A ENSP00000501203.1:p.Val30Met
ENST00000361487.6:c.88G>A ENSP00000355245.6:p.Val30Met
ENST00000402703.6:c.88G>A ENSP00000384817.2:p.Val30Met
ENST00000554201.1:c.-474G>A ENSP00000450434.1:n.-474G>A
ENST00000555639.1:n.390G>A
NM_006194.3:c.88G>A NP_006185.1:p.Val30Met
NM_001372076.1:c.88G>A MANE Select NP_001359005.1:p.Val30Met
NM_006194.4:c.88G>A NP_006185.1:p.Val30Met
Search 100 bp 5'
Search 100 bp 3'