Canonical Allele Identifier: CA418189014
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739506
MyVariant Identifiers: chr1:g.59248311A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782639A>G , CM000663.2:g.58782639A>G GRCh38
NC_000001.10:g.59248311A>G , CM000663.1:g.59248311A>G GRCh37
NC_000001.9:g.59020899A>G NCBI36
NG_047027.1:g.6475T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.498T>C ENSP00000518166.1:p.Ala166=
ENST00000371222.4:c.432T>C MANE Select ENSP00000360266.2:p.Ala144=
ENST00000678696.1:c.432T>C ENSP00000503132.1:p.Ala144=
ENST00000371222.3:c.432T>C ENSP00000360266.2:p.Ala144=
NM_002228.3:c.432T>C NP_002219.1:p.Ala144=
NM_002228.4:c.432T>C MANE Select NP_002219.1:p.Ala144=