Canonical Allele Identifier: CA340578122
Gene: JUN HGNC NCBI

Linked Data

gnomAD v4: 1-58782539-G-T
MyVariant Identifiers: chr1:g.59248211G>T (hg19) chr1:g.58782539G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782539G>T , CM000663.2:g.58782539G>T GRCh38
NC_000001.10:g.59248211G>T , CM000663.1:g.59248211G>T GRCh37
NC_000001.9:g.59020799G>T NCBI36
NG_047027.1:g.6575C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.598C>A ENSP00000518166.1:p.Pro200Thr
ENST00000371222.4:c.532C>A MANE Select ENSP00000360266.2:p.Pro178Thr
ENST00000678696.1:c.532C>A ENSP00000503132.1:p.Pro178Thr
ENST00000371222.3:c.532C>A ENSP00000360266.2:p.Pro178Thr
NM_002228.3:c.532C>A NP_002219.1:p.Pro178Thr
NM_002228.4:c.532C>A MANE Select NP_002219.1:p.Pro178Thr
Search 100 bp 5'
Search 100 bp 3'