Canonical Allele Identifier: CA418189087
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248362C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782690C>A , CM000663.2:g.58782690C>A GRCh38
NC_000001.10:g.59248362C>A , CM000663.1:g.59248362C>A GRCh37
NC_000001.9:g.59020950C>A NCBI36
NG_047027.1:g.6424G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.447G>T ENSP00000518166.1:p.Leu149=
ENST00000371222.4:c.381G>T MANE Select ENSP00000360266.2:p.Leu127=
ENST00000678696.1:c.381G>T ENSP00000503132.1:p.Leu127=
ENST00000371222.3:c.381G>T ENSP00000360266.2:p.Leu127=
NM_002228.3:c.381G>T NP_002219.1:p.Leu127=
NM_002228.4:c.381G>T MANE Select NP_002219.1:p.Leu127=