Canonical Allele Identifier: CA340578188
Gene: JUN HGNC NCBI

Linked Data

gnomAD v4: 1-58782568-G-T
MyVariant Identifiers: chr1:g.59248240G>T (hg19) chr1:g.58782568G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782568G>T , CM000663.2:g.58782568G>T GRCh38
NC_000001.10:g.59248240G>T , CM000663.1:g.59248240G>T GRCh37
NC_000001.9:g.59020828G>T NCBI36
NG_047027.1:g.6546C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.569C>A ENSP00000518166.1:p.Pro190Gln
ENST00000371222.4:c.503C>A MANE Select ENSP00000360266.2:p.Pro168Gln
ENST00000678696.1:c.503C>A ENSP00000503132.1:p.Pro168Gln
ENST00000371222.3:c.503C>A ENSP00000360266.2:p.Pro168Gln
NM_002228.3:c.503C>A NP_002219.1:p.Pro168Gln
NM_002228.4:c.503C>A MANE Select NP_002219.1:p.Pro168Gln
Search 100 bp 5'
Search 100 bp 3'