Canonical Allele Identifier: CA340577446
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100738738

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782227C>T , CM000663.2:g.58782227C>T GRCh38
NC_000001.10:g.59247899C>T , CM000663.1:g.59247899C>T GRCh37
NC_000001.9:g.59020487C>T NCBI36
NG_047027.1:g.6887G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000710273.1:c.910G>A ENSP00000518166.1:p.Glu304Lys
ENST00000371222.4:c.844G>A MANE Select ENSP00000360266.2:p.Glu282Lys
ENST00000678696.1:c.844G>A ENSP00000503132.1:p.Glu282Lys
ENST00000371222.3:c.844G>A ENSP00000360266.2:p.Glu282Lys
NM_002228.3:c.844G>A NP_002219.1:p.Glu282Lys
NM_002228.4:c.844G>A MANE Select NP_002219.1:p.Glu282Lys