Canonical Allele Identifier: CA418189121
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248389C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782717C>T , CM000663.2:g.58782717C>T GRCh38
NC_000001.10:g.59248389C>T , CM000663.1:g.59248389C>T GRCh37
NC_000001.9:g.59020977C>T NCBI36
NG_047027.1:g.6397G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.420G>A ENSP00000518166.1:p.Leu140=
ENST00000371222.4:c.354G>A MANE Select ENSP00000360266.2:p.Leu118=
ENST00000678696.1:c.354G>A ENSP00000503132.1:p.Leu118=
ENST00000371222.3:c.354G>A ENSP00000360266.2:p.Leu118=
NM_002228.3:c.354G>A NP_002219.1:p.Leu118=
NM_002228.4:c.354G>A MANE Select NP_002219.1:p.Leu118=