Canonical Allele Identifier: CA418188723
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1645586970
MyVariant Identifiers: chr1:g.59248407C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782735C>T , CM000663.2:g.58782735C>T GRCh38
NC_000001.10:g.59248407C>T , CM000663.1:g.59248407C>T GRCh37
NC_000001.9:g.59020995C>T NCBI36
NG_047027.1:g.6379G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.402G>A ENSP00000518166.1:p.Glu134=
ENST00000371222.4:c.336G>A MANE Select ENSP00000360266.2:p.Glu112=
ENST00000678696.1:c.336G>A ENSP00000503132.1:p.Glu112=
ENST00000371222.3:c.336G>A ENSP00000360266.2:p.Glu112=
NM_002228.3:c.336G>A NP_002219.1:p.Glu112=
NM_002228.4:c.336G>A MANE Select NP_002219.1:p.Glu112=