Canonical Allele Identifier: CA878299
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs551506166
ExAC: 1:59248169 C / T
gnomAD v2: 1-59248169-C-T
gnomAD v4: 1-58782497-C-T
MyVariant Identifiers: chr1:g.59248169C>T (hg19) chr1:g.58782497C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782497C>T , CM000663.2:g.58782497C>T GRCh38
NC_000001.10:g.59248169C>T , CM000663.1:g.59248169C>T GRCh37
NC_000001.9:g.59020757C>T NCBI36
NG_047027.1:g.6617G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.640G>A ENSP00000518166.1:p.Ala214Thr
ENST00000371222.4:c.574G>A MANE Select ENSP00000360266.2:p.Ala192Thr
ENST00000678696.1:c.574G>A ENSP00000503132.1:p.Ala192Thr
ENST00000371222.3:c.574G>A ENSP00000360266.2:p.Ala192Thr
NM_002228.3:c.574G>A NP_002219.1:p.Ala192Thr
NM_002228.4:c.574G>A MANE Select NP_002219.1:p.Ala192Thr
Search 100 bp 5'
Search 100 bp 3'