Canonical Allele Identifier: CA878301
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs745564110
ExAC: 1:59248182 C / T
gnomAD v2: 1-59248182-C-T
gnomAD v4: 1-58782510-C-T
MyVariant Identifiers: chr1:g.59248182C>T (hg19) chr1:g.58782510C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782510C>T , CM000663.2:g.58782510C>T GRCh38
NC_000001.10:g.59248182C>T , CM000663.1:g.59248182C>T GRCh37
NC_000001.9:g.59020770C>T NCBI36
NG_047027.1:g.6604G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.627G>A ENSP00000518166.1:p.Ala209=
ENST00000371222.4:c.561G>A MANE Select ENSP00000360266.2:p.Ala187=
ENST00000678696.1:c.561G>A ENSP00000503132.1:p.Ala187=
ENST00000371222.3:c.561G>A ENSP00000360266.2:p.Ala187=
NM_002228.3:c.561G>A NP_002219.1:p.Ala187=
NM_002228.4:c.561G>A MANE Select NP_002219.1:p.Ala187=
Search 100 bp 5'
Search 100 bp 3'