Canonical Allele Identifier: CA340578498
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739666
gnomAD v4: 1-58782721-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782721G>A , CM000663.2:g.58782721G>A GRCh38
NC_000001.10:g.59248393G>A , CM000663.1:g.59248393G>A GRCh37
NC_000001.9:g.59020981G>A NCBI36
NG_047027.1:g.6393C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.416C>T ENSP00000518166.1:p.Ala139Val
ENST00000371222.4:c.350C>T MANE Select ENSP00000360266.2:p.Ala117Val
ENST00000678696.1:c.350C>T ENSP00000503132.1:p.Ala117Val
ENST00000371222.3:c.350C>T ENSP00000360266.2:p.Ala117Val
NM_002228.3:c.350C>T NP_002219.1:p.Ala117Val
NM_002228.4:c.350C>T MANE Select NP_002219.1:p.Ala117Val