Canonical Allele Identifier: CA878288
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs763958620
ExAC: 1:59248126 T / C
gnomAD v2: 1-59248126-T-C
gnomAD v3: 1-58782454-T-C
gnomAD v4: 1-58782454-T-C
MyVariant Identifiers: chr1:g.59248126T>C (hg19) chr1:g.58782454T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782454T>C , CM000663.2:g.58782454T>C GRCh38
NC_000001.10:g.59248126T>C , CM000663.1:g.59248126T>C GRCh37
NC_000001.9:g.59020714T>C NCBI36
NG_047027.1:g.6660A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.683A>G ENSP00000518166.1:p.Gln228Arg
ENST00000371222.4:c.617A>G MANE Select ENSP00000360266.2:p.Gln206Arg
ENST00000678696.1:c.617A>G ENSP00000503132.1:p.Gln206Arg
ENST00000371222.3:c.617A>G ENSP00000360266.2:p.Gln206Arg
NM_002228.3:c.617A>G NP_002219.1:p.Gln206Arg
NM_002228.4:c.617A>G MANE Select NP_002219.1:p.Gln206Arg
Search 100 bp 5'
Search 100 bp 3'