Canonical Allele Identifier: CA878332
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs200708109
ExAC: 1:59248339 T / C
gnomAD v2: 1-59248339-T-C
gnomAD v3: 1-58782667-T-C
gnomAD v4: 1-58782667-T-C
MyVariant Identifiers: chr1:g.59248339T>C (hg19) chr1:g.58782667T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782667T>C , CM000663.2:g.58782667T>C GRCh38
NC_000001.10:g.59248339T>C , CM000663.1:g.59248339T>C GRCh37
NC_000001.9:g.59020927T>C NCBI36
NG_047027.1:g.6447A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.470A>G ENSP00000518166.1:p.Gln157Arg
ENST00000371222.4:c.404A>G MANE Select ENSP00000360266.2:p.Gln135Arg
ENST00000678696.1:c.404A>G ENSP00000503132.1:p.Gln135Arg
ENST00000371222.3:c.404A>G ENSP00000360266.2:p.Gln135Arg
NM_002228.3:c.404A>G NP_002219.1:p.Gln135Arg
NM_002228.4:c.404A>G MANE Select NP_002219.1:p.Gln135Arg
Search 100 bp 5'
Search 100 bp 3'