Canonical Allele Identifier: CA418188718
Gene: JUN HGNC NCBI

Linked Data

gnomAD v4: 1-58782468-G-T
MyVariant Identifiers: chr1:g.59248140G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782468G>T , CM000663.2:g.58782468G>T GRCh38
NC_000001.10:g.59248140G>T , CM000663.1:g.59248140G>T GRCh37
NC_000001.9:g.59020728G>T NCBI36
NG_047027.1:g.6646C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.669C>A ENSP00000518166.1:p.Pro223=
ENST00000371222.4:c.603C>A MANE Select ENSP00000360266.2:p.Pro201=
ENST00000678696.1:c.603C>A ENSP00000503132.1:p.Pro201=
ENST00000371222.3:c.603C>A ENSP00000360266.2:p.Pro201=
NM_002228.3:c.603C>A NP_002219.1:p.Pro201=
NM_002228.4:c.603C>A MANE Select NP_002219.1:p.Pro201=