Canonical Allele Identifier: CA418188716
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739128
gnomAD v4: 1-58782468-G-A
MyVariant Identifiers: chr1:g.59248140G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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