Canonical Allele Identifier: CA418188513
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100738746
MyVariant Identifiers: chr1:g.59247903C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782231C>T , CM000663.2:g.58782231C>T GRCh38
NC_000001.10:g.59247903C>T , CM000663.1:g.59247903C>T GRCh37
NC_000001.9:g.59020491C>T NCBI36
NG_047027.1:g.6883G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000710273.1:c.906G>A ENSP00000518166.1:p.Leu302=
ENST00000371222.4:c.840G>A MANE Select ENSP00000360266.2:p.Leu280=
ENST00000678696.1:c.840G>A ENSP00000503132.1:p.Leu280=
ENST00000371222.3:c.840G>A ENSP00000360266.2:p.Leu280=
NM_002228.3:c.840G>A NP_002219.1:p.Leu280=
NM_002228.4:c.840G>A MANE Select NP_002219.1:p.Leu280=
Search 100 bp 5'
Search 100 bp 3'