Canonical Allele Identifier: CA340578215
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248252T>C (hg19) chr1:g.58782580T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782580T>C , CM000663.2:g.58782580T>C GRCh38
NC_000001.10:g.59248252T>C , CM000663.1:g.59248252T>C GRCh37
NC_000001.9:g.59020840T>C NCBI36
NG_047027.1:g.6534A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.557A>G ENSP00000518166.1:p.His186Arg
ENST00000371222.4:c.491A>G MANE Select ENSP00000360266.2:p.His164Arg
ENST00000678696.1:c.491A>G ENSP00000503132.1:p.His164Arg
ENST00000371222.3:c.491A>G ENSP00000360266.2:p.His164Arg
NM_002228.3:c.491A>G NP_002219.1:p.His164Arg
NM_002228.4:c.491A>G MANE Select NP_002219.1:p.His164Arg
Search 100 bp 5'
Search 100 bp 3'