Canonical Allele Identifier: CA340578171
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739327
gnomAD v4: 1-58782560-C-T
MyVariant Identifiers: chr1:g.59248232C>T (hg19) chr1:g.58782560C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782560C>T , CM000663.2:g.58782560C>T GRCh38
NC_000001.10:g.59248232C>T , CM000663.1:g.59248232C>T GRCh37
NC_000001.9:g.59020820C>T NCBI36
NG_047027.1:g.6554G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.577G>A ENSP00000518166.1:p.Ala193Thr
ENST00000371222.4:c.511G>A MANE Select ENSP00000360266.2:p.Ala171Thr
ENST00000678696.1:c.511G>A ENSP00000503132.1:p.Ala171Thr
ENST00000371222.3:c.511G>A ENSP00000360266.2:p.Ala171Thr
NM_002228.3:c.511G>A NP_002219.1:p.Ala171Thr
NM_002228.4:c.511G>A MANE Select NP_002219.1:p.Ala171Thr
Search 100 bp 5'
Search 100 bp 3'