Canonical Allele Identifier: CA389466578
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132413C>A (hg19) chr14:g.36663208C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663208C>A , CM000676.2:g.36663208C>A GRCh38
NC_000014.8:g.37132413C>A , CM000676.1:g.37132413C>A GRCh37
NC_000014.7:g.36202164C>A NCBI36
NG_013357.1:g.10641C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.316C>A MANE Select ENSP00000355245.6:p.Leu106Met
ENST00000361487.6:c.316C>A ENSP00000355245.6:p.Leu106Met
ENST00000402703.6:c.316C>A ENSP00000384817.2:p.Leu106Met
ENST00000554201.1:c.-246C>A ENSP00000450434.1:n.-246C>A
NM_006194.3:c.316C>A NP_006185.1:p.Leu106Met
NM_001372076.1:c.316C>A MANE Select NP_001359005.1:p.Leu106Met
NM_006194.4:c.316C>A NP_006185.1:p.Leu106Met
Search 100 bp 5'
Search 100 bp 3'