Canonical Allele Identifier: CA389466350
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132309T>A (hg19) chr14:g.36663104T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663104T>A , CM000676.2:g.36663104T>A GRCh38
NC_000014.8:g.37132309T>A , CM000676.1:g.37132309T>A GRCh37
NC_000014.7:g.36202060T>A NCBI36
NG_013357.1:g.10537T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.212T>A MANE Select ENSP00000355245.6:p.Ile71Asn
ENST00000555639.2:c.212T>A ENSP00000501203.1:p.Ile71Asn
ENST00000361487.6:c.212T>A ENSP00000355245.6:p.Ile71Asn
ENST00000402703.6:c.212T>A ENSP00000384817.2:p.Ile71Asn
ENST00000554201.1:c.-350T>A ENSP00000450434.1:n.-350T>A
ENST00000555639.1:n.514T>A
NM_006194.3:c.212T>A NP_006185.1:p.Ile71Asn
NM_001372076.1:c.212T>A MANE Select NP_001359005.1:p.Ile71Asn
NM_006194.4:c.212T>A NP_006185.1:p.Ile71Asn
Search 100 bp 5'
Search 100 bp 3'