Canonical Allele Identifier: CA340578502
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1329490786
gnomAD v2: 1-59248394-C-T
gnomAD v4: 1-58782722-C-T
MyVariant Identifiers: chr1:g.59248394C>T (hg19) chr1:g.58782722C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782722C>T , CM000663.2:g.58782722C>T GRCh38
NC_000001.10:g.59248394C>T , CM000663.1:g.59248394C>T GRCh37
NC_000001.9:g.59020982C>T NCBI36
NG_047027.1:g.6392G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.415G>A ENSP00000518166.1:p.Ala139Thr
ENST00000371222.4:c.349G>A MANE Select ENSP00000360266.2:p.Ala117Thr
ENST00000678696.1:c.349G>A ENSP00000503132.1:p.Ala117Thr
ENST00000371222.3:c.349G>A ENSP00000360266.2:p.Ala117Thr
NM_002228.3:c.349G>A NP_002219.1:p.Ala117Thr
NM_002228.4:c.349G>A MANE Select NP_002219.1:p.Ala117Thr
Search 100 bp 5'
Search 100 bp 3'