Canonical Allele Identifier: CA418188912
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1377912249
gnomAD v2: 1-59248242-C-T
gnomAD v4: 1-58782570-C-T
MyVariant Identifiers: chr1:g.59248242C>T (hg19) chr1:g.58782570C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782570C>T , CM000663.2:g.58782570C>T GRCh38
NC_000001.10:g.59248242C>T , CM000663.1:g.59248242C>T GRCh37
NC_000001.9:g.59020830C>T NCBI36
NG_047027.1:g.6544G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.567G>A ENSP00000518166.1:p.Pro189=
ENST00000371222.4:c.501G>A MANE Select ENSP00000360266.2:p.Pro167=
ENST00000678696.1:c.501G>A ENSP00000503132.1:p.Pro167=
ENST00000371222.3:c.501G>A ENSP00000360266.2:p.Pro167=
NM_002228.3:c.501G>A NP_002219.1:p.Pro167=
NM_002228.4:c.501G>A MANE Select NP_002219.1:p.Pro167=
Search 100 bp 5'
Search 100 bp 3'