Canonical Allele Identifier: CA878277
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs776316570
ExAC: 1:59248098 C / T
gnomAD v2: 1-59248098-C-T
gnomAD v3: 1-58782426-C-T
gnomAD v4: 1-58782426-C-T
MyVariant Identifiers: chr1:g.59248098C>T (hg19) chr1:g.58782426C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782426C>T , CM000663.2:g.58782426C>T GRCh38
NC_000001.10:g.59248098C>T , CM000663.1:g.59248098C>T GRCh37
NC_000001.9:g.59020686C>T NCBI36
NG_047027.1:g.6688G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.711G>A ENSP00000518166.1:p.Met237Ile
ENST00000371222.4:c.645G>A MANE Select ENSP00000360266.2:p.Met215Ile
ENST00000678696.1:c.645G>A ENSP00000503132.1:p.Met215Ile
ENST00000371222.3:c.645G>A ENSP00000360266.2:p.Met215Ile
NM_002228.3:c.645G>A NP_002219.1:p.Met215Ile
NM_002228.4:c.645G>A MANE Select NP_002219.1:p.Met215Ile
Search 100 bp 5'
Search 100 bp 3'