Canonical Allele Identifier: CA340578182
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1471498107
gnomAD v2: 1-59248237-A-T
gnomAD v3: 1-58782565-A-T
gnomAD v4: 1-58782565-A-T
MyVariant Identifiers: chr1:g.59248237A>T (hg19) chr1:g.58782565A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782565A>T , CM000663.2:g.58782565A>T GRCh38
NC_000001.10:g.59248237A>T , CM000663.1:g.59248237A>T GRCh37
NC_000001.9:g.59020825A>T NCBI36
NG_047027.1:g.6549T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.572T>A ENSP00000518166.1:p.Val191Asp
ENST00000371222.4:c.506T>A MANE Select ENSP00000360266.2:p.Val169Asp
ENST00000678696.1:c.506T>A ENSP00000503132.1:p.Val169Asp
ENST00000371222.3:c.506T>A ENSP00000360266.2:p.Val169Asp
NM_002228.3:c.506T>A NP_002219.1:p.Val169Asp
NM_002228.4:c.506T>A MANE Select NP_002219.1:p.Val169Asp
Search 100 bp 5'
Search 100 bp 3'