Canonical Allele Identifier: CA418188756
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs748565775
gnomAD v4: 1-58782495-C-A
MyVariant Identifiers: chr1:g.59248167C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782495C>A , CM000663.2:g.58782495C>A GRCh38
NC_000001.10:g.59248167C>A , CM000663.1:g.59248167C>A GRCh37
NC_000001.9:g.59020755C>A NCBI36
NG_047027.1:g.6619G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.642G>T ENSP00000518166.1:p.Ala214=
ENST00000371222.4:c.576G>T MANE Select ENSP00000360266.2:p.Ala192=
ENST00000678696.1:c.576G>T ENSP00000503132.1:p.Ala192=
ENST00000371222.3:c.576G>T ENSP00000360266.2:p.Ala192=
NM_002228.3:c.576G>T NP_002219.1:p.Ala192=
NM_002228.4:c.576G>T MANE Select NP_002219.1:p.Ala192=