Canonical Allele Identifier: CA340578355
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs771850245
gnomAD v4: 1-58782649-C-T
MyVariant Identifiers: chr1:g.59248321C>T (hg19) chr1:g.58782649C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782649C>T , CM000663.2:g.58782649C>T GRCh38
NC_000001.10:g.59248321C>T , CM000663.1:g.59248321C>T GRCh37
NC_000001.9:g.59020909C>T NCBI36
NG_047027.1:g.6465G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.488G>A ENSP00000518166.1:p.Gly163Asp
ENST00000371222.4:c.422G>A MANE Select ENSP00000360266.2:p.Gly141Asp
ENST00000678696.1:c.422G>A ENSP00000503132.1:p.Gly141Asp
ENST00000371222.3:c.422G>A ENSP00000360266.2:p.Gly141Asp
NM_002228.3:c.422G>A NP_002219.1:p.Gly141Asp
NM_002228.4:c.422G>A MANE Select NP_002219.1:p.Gly141Asp
Search 100 bp 5'
Search 100 bp 3'