Canonical Allele Identifier: CA878339
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs754560735
ExAC: 1:59248366 G / T
gnomAD v2: 1-59248366-G-T
gnomAD v4: 1-58782694-G-T
MyVariant Identifiers: chr1:g.59248366G>T (hg19) chr1:g.58782694G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782694G>T , CM000663.2:g.58782694G>T GRCh38
NC_000001.10:g.59248366G>T , CM000663.1:g.59248366G>T GRCh37
NC_000001.9:g.59020954G>T NCBI36
NG_047027.1:g.6420C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.443C>A ENSP00000518166.1:p.Thr148Lys
ENST00000371222.4:c.377C>A MANE Select ENSP00000360266.2:p.Thr126Lys
ENST00000678696.1:c.377C>A ENSP00000503132.1:p.Thr126Lys
ENST00000371222.3:c.377C>A ENSP00000360266.2:p.Thr126Lys
NM_002228.3:c.377C>A NP_002219.1:p.Thr126Lys
NM_002228.4:c.377C>A MANE Select NP_002219.1:p.Thr126Lys
Search 100 bp 5'
Search 100 bp 3'