Canonical Allele Identifier: CA418188795
Gene: JUN HGNC NCBI

Linked Data

gnomAD v4: 1-58782513-C-T
MyVariant Identifiers: chr1:g.59248185C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782513C>T , CM000663.2:g.58782513C>T GRCh38
NC_000001.10:g.59248185C>T , CM000663.1:g.59248185C>T GRCh37
NC_000001.9:g.59020773C>T NCBI36
NG_047027.1:g.6601G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.624G>A ENSP00000518166.1:p.Gly208=
ENST00000371222.4:c.558G>A MANE Select ENSP00000360266.2:p.Gly186=
ENST00000678696.1:c.558G>A ENSP00000503132.1:p.Gly186=
ENST00000371222.3:c.558G>A ENSP00000360266.2:p.Gly186=
NM_002228.3:c.558G>A NP_002219.1:p.Gly186=
NM_002228.4:c.558G>A MANE Select NP_002219.1:p.Gly186=
Search 100 bp 5'
Search 100 bp 3'