Canonical Allele Identifier: CA878323
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs760060765
gnomAD v2: 1-59248310-G-A
gnomAD v4: 1-58782638-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782638G>A , CM000663.2:g.58782638G>A GRCh38
NC_000001.10:g.59248310G>A , CM000663.1:g.59248310G>A GRCh37
NC_000001.9:g.59020898G>A NCBI36
NG_047027.1:g.6476C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.499C>T ENSP00000518166.1:p.Pro167Ser
ENST00000371222.4:c.433C>T MANE Select ENSP00000360266.2:p.Pro145Ser
ENST00000678696.1:c.433C>T ENSP00000503132.1:p.Pro145Ser
ENST00000371222.3:c.433C>T ENSP00000360266.2:p.Pro145Ser
NM_002228.3:c.433C>T NP_002219.1:p.Pro145Ser
NM_002228.4:c.433C>T MANE Select NP_002219.1:p.Pro145Ser