Canonical Allele Identifier: CA418189063
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248347C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782675C>G , CM000663.2:g.58782675C>G GRCh38
NC_000001.10:g.59248347C>G , CM000663.1:g.59248347C>G GRCh37
NC_000001.9:g.59020935C>G NCBI36
NG_047027.1:g.6439G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.462G>C ENSP00000518166.1:p.Ser154=
ENST00000371222.4:c.396G>C MANE Select ENSP00000360266.2:p.Ser132=
ENST00000678696.1:c.396G>C ENSP00000503132.1:p.Ser132=
ENST00000371222.3:c.396G>C ENSP00000360266.2:p.Ser132=
NM_002228.3:c.396G>C NP_002219.1:p.Ser132=
NM_002228.4:c.396G>C MANE Select NP_002219.1:p.Ser132=