Canonical Allele Identifier: CA878290
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs761589638
ExAC: 1:59248134 C / T
gnomAD v2: 1-59248134-C-T
gnomAD v4: 1-58782462-C-T
MyVariant Identifiers: chr1:g.59248134C>T (hg19) chr1:g.58782462C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782462C>T , CM000663.2:g.58782462C>T GRCh38
NC_000001.10:g.59248134C>T , CM000663.1:g.59248134C>T GRCh37
NC_000001.9:g.59020722C>T NCBI36
NG_047027.1:g.6652G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.675G>A ENSP00000518166.1:p.Gln225=
ENST00000371222.4:c.609G>A MANE Select ENSP00000360266.2:p.Gln203=
ENST00000678696.1:c.609G>A ENSP00000503132.1:p.Gln203=
ENST00000371222.3:c.609G>A ENSP00000360266.2:p.Gln203=
NM_002228.3:c.609G>A NP_002219.1:p.Gln203=
NM_002228.4:c.609G>A MANE Select NP_002219.1:p.Gln203=
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