Canonical Allele Identifier: CA878337
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs779728211
gnomAD v2: 1-59248357-C-T
gnomAD v3: 1-58782685-C-T
gnomAD v4: 1-58782685-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782685C>T , CM000663.2:g.58782685C>T GRCh38
NC_000001.10:g.59248357C>T , CM000663.1:g.59248357C>T GRCh37
NC_000001.9:g.59020945C>T NCBI36
NG_047027.1:g.6429G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.452G>A ENSP00000518166.1:p.Ser151Asn
ENST00000371222.4:c.386G>A MANE Select ENSP00000360266.2:p.Ser129Asn
ENST00000678696.1:c.386G>A ENSP00000503132.1:p.Ser129Asn
ENST00000371222.3:c.386G>A ENSP00000360266.2:p.Ser129Asn
NM_002228.3:c.386G>A NP_002219.1:p.Ser129Asn
NM_002228.4:c.386G>A MANE Select NP_002219.1:p.Ser129Asn