Canonical Allele Identifier: CA418188711
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739676
gnomAD v4: 1-58782726-C-A
MyVariant Identifiers: chr1:g.59248398C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782726C>A , CM000663.2:g.58782726C>A GRCh38
NC_000001.10:g.59248398C>A , CM000663.1:g.59248398C>A GRCh37
NC_000001.9:g.59020986C>A NCBI36
NG_047027.1:g.6388G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.411G>T ENSP00000518166.1:p.Val137=
ENST00000371222.4:c.345G>T MANE Select ENSP00000360266.2:p.Val115=
ENST00000678696.1:c.345G>T ENSP00000503132.1:p.Val115=
ENST00000371222.3:c.345G>T ENSP00000360266.2:p.Val115=
NM_002228.3:c.345G>T NP_002219.1:p.Val115=
NM_002228.4:c.345G>T MANE Select NP_002219.1:p.Val115=