Canonical Allele Identifier: CA418188968
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1645585417
gnomAD v4: 1-58782612-G-A
MyVariant Identifiers: chr1:g.59248284G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782612G>A , CM000663.2:g.58782612G>A GRCh38
NC_000001.10:g.59248284G>A , CM000663.1:g.59248284G>A GRCh37
NC_000001.9:g.59020872G>A NCBI36
NG_047027.1:g.6502C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.525C>T ENSP00000518166.1:p.Gly175=
ENST00000371222.4:c.459C>T MANE Select ENSP00000360266.2:p.Gly153=
ENST00000678696.1:c.459C>T ENSP00000503132.1:p.Gly153=
ENST00000371222.3:c.459C>T ENSP00000360266.2:p.Gly153=
NM_002228.3:c.459C>T NP_002219.1:p.Gly153=
NM_002228.4:c.459C>T MANE Select NP_002219.1:p.Gly153=