Canonical Allele Identifier: CA340578519
Gene: JUN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782730A>T , CM000663.2:g.58782730A>T GRCh38
NC_000001.10:g.59248402A>T , CM000663.1:g.59248402A>T GRCh37
NC_000001.9:g.59020990A>T NCBI36
NG_047027.1:g.6384T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.407T>A ENSP00000518166.1:p.Phe136Tyr
ENST00000371222.4:c.341T>A MANE Select ENSP00000360266.2:p.Phe114Tyr
ENST00000678696.1:c.341T>A ENSP00000503132.1:p.Phe114Tyr
ENST00000371222.3:c.341T>A ENSP00000360266.2:p.Phe114Tyr
NM_002228.3:c.341T>A NP_002219.1:p.Phe114Tyr
NM_002228.4:c.341T>A MANE Select NP_002219.1:p.Phe114Tyr