Canonical Allele Identifier: CA418188701
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs769366357
gnomAD v4: 1-58782447-C-A
MyVariant Identifiers: chr1:g.59248119C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782447C>A , CM000663.2:g.58782447C>A GRCh38
NC_000001.10:g.59248119C>A , CM000663.1:g.59248119C>A GRCh37
NC_000001.9:g.59020707C>A NCBI36
NG_047027.1:g.6667G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.690G>T ENSP00000518166.1:p.Pro230=
ENST00000371222.4:c.624G>T MANE Select ENSP00000360266.2:p.Pro208=
ENST00000678696.1:c.624G>T ENSP00000503132.1:p.Pro208=
ENST00000371222.3:c.624G>T ENSP00000360266.2:p.Pro208=
NM_002228.3:c.624G>T NP_002219.1:p.Pro208=
NM_002228.4:c.624G>T MANE Select NP_002219.1:p.Pro208=