Canonical Allele Identifier: CA878291
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs559705593
gnomAD v2: 1-59248138-T-G
gnomAD v3: 1-58782466-T-G
gnomAD v4: 1-58782466-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782466T>G , CM000663.2:g.58782466T>G GRCh38
NC_000001.10:g.59248138T>G , CM000663.1:g.59248138T>G GRCh37
NC_000001.9:g.59020726T>G NCBI36
NG_047027.1:g.6648A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.671A>C ENSP00000518166.1:p.Gln224Pro
ENST00000371222.4:c.605A>C MANE Select ENSP00000360266.2:p.Gln202Pro
ENST00000678696.1:c.605A>C ENSP00000503132.1:p.Gln202Pro
ENST00000371222.3:c.605A>C ENSP00000360266.2:p.Gln202Pro
NM_002228.3:c.605A>C NP_002219.1:p.Gln202Pro
NM_002228.4:c.605A>C MANE Select NP_002219.1:p.Gln202Pro