Canonical Allele Identifier: CA389466455
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132357T>G (hg19) chr14:g.36663152T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663152T>G , CM000676.2:g.36663152T>G GRCh38
NC_000014.8:g.37132357T>G , CM000676.1:g.37132357T>G GRCh37
NC_000014.7:g.36202108T>G NCBI36
NG_013357.1:g.10585T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.260T>G MANE Select ENSP00000355245.6:p.Ile87Ser
ENST00000361487.6:c.260T>G ENSP00000355245.6:p.Ile87Ser
ENST00000402703.6:c.260T>G ENSP00000384817.2:p.Ile87Ser
ENST00000554201.1:c.-302T>G ENSP00000450434.1:n.-302T>G
NM_006194.3:c.260T>G NP_006185.1:p.Ile87Ser
NM_001372076.1:c.260T>G MANE Select NP_001359005.1:p.Ile87Ser
NM_006194.4:c.260T>G NP_006185.1:p.Ile87Ser
Search 100 bp 5'
Search 100 bp 3'