Canonical Allele Identifier: CA418188751
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs779558859
gnomAD v4: 1-58782492-G-A
MyVariant Identifiers: chr1:g.59248164G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782492G>A , CM000663.2:g.58782492G>A GRCh38
NC_000001.10:g.59248164G>A , CM000663.1:g.59248164G>A GRCh37
NC_000001.9:g.59020752G>A NCBI36
NG_047027.1:g.6622C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.645C>T ENSP00000518166.1:p.Ala215=
ENST00000371222.4:c.579C>T MANE Select ENSP00000360266.2:p.Ala193=
ENST00000678696.1:c.579C>T ENSP00000503132.1:p.Ala193=
ENST00000371222.3:c.579C>T ENSP00000360266.2:p.Ala193=
NM_002228.3:c.579C>T NP_002219.1:p.Ala193=
NM_002228.4:c.579C>T MANE Select NP_002219.1:p.Ala193=