Canonical Allele Identifier: CA340578359
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248322C>T (hg19) chr1:g.58782650C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782650C>T , CM000663.2:g.58782650C>T GRCh38
NC_000001.10:g.59248322C>T , CM000663.1:g.59248322C>T GRCh37
NC_000001.9:g.59020910C>T NCBI36
NG_047027.1:g.6464G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.487G>A ENSP00000518166.1:p.Gly163Ser
ENST00000371222.4:c.421G>A MANE Select ENSP00000360266.2:p.Gly141Ser
ENST00000678696.1:c.421G>A ENSP00000503132.1:p.Gly141Ser
ENST00000371222.3:c.421G>A ENSP00000360266.2:p.Gly141Ser
NM_002228.3:c.421G>A NP_002219.1:p.Gly141Ser
NM_002228.4:c.421G>A MANE Select NP_002219.1:p.Gly141Ser
Search 100 bp 5'
Search 100 bp 3'