Canonical Allele Identifier: CA418188515
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59247905G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782233G>A , CM000663.2:g.58782233G>A GRCh38
NC_000001.10:g.59247905G>A , CM000663.1:g.59247905G>A GRCh37
NC_000001.9:g.59020493G>A NCBI36
NG_047027.1:g.6881C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710273.1:c.904C>T ENSP00000518166.1:p.Leu302=
ENST00000371222.4:c.838C>T MANE Select ENSP00000360266.2:p.Leu280=
ENST00000678696.1:c.838C>T ENSP00000503132.1:p.Leu280=
ENST00000371222.3:c.838C>T ENSP00000360266.2:p.Leu280=
NM_002228.3:c.838C>T NP_002219.1:p.Leu280=
NM_002228.4:c.838C>T MANE Select NP_002219.1:p.Leu280=