Canonical Allele Identifier: CA878335
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs573002199
ExAC: 1:59248354 A / G
gnomAD v2: 1-59248354-A-G
gnomAD v3: 1-58782682-A-G
gnomAD v4: 1-58782682-A-G
MyVariant Identifiers: chr1:g.59248354A>G (hg19) chr1:g.58782682A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782682A>G , CM000663.2:g.58782682A>G GRCh38
NC_000001.10:g.59248354A>G , CM000663.1:g.59248354A>G GRCh37
NC_000001.9:g.59020942A>G NCBI36
NG_047027.1:g.6432T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.455T>C ENSP00000518166.1:p.Val152Ala
ENST00000371222.4:c.389T>C MANE Select ENSP00000360266.2:p.Val130Ala
ENST00000678696.1:c.389T>C ENSP00000503132.1:p.Val130Ala
ENST00000371222.3:c.389T>C ENSP00000360266.2:p.Val130Ala
NM_002228.3:c.389T>C NP_002219.1:p.Val130Ala
NM_002228.4:c.389T>C MANE Select NP_002219.1:p.Val130Ala
Search 100 bp 5'
Search 100 bp 3'