Canonical Allele Identifier: CA878308
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs767378953
ExAC: 1:59248220 T / C
gnomAD v2: 1-59248220-T-C
gnomAD v3: 1-58782548-T-C
gnomAD v4: 1-58782548-T-C
MyVariant Identifiers: chr1:g.59248220T>C (hg19) chr1:g.58782548T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782548T>C , CM000663.2:g.58782548T>C GRCh38
NC_000001.10:g.59248220T>C , CM000663.1:g.59248220T>C GRCh37
NC_000001.9:g.59020808T>C NCBI36
NG_047027.1:g.6566A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.589A>G ENSP00000518166.1:p.Asn197Asp
ENST00000371222.4:c.523A>G MANE Select ENSP00000360266.2:p.Asn175Asp
ENST00000678696.1:c.523A>G ENSP00000503132.1:p.Asn175Asp
ENST00000371222.3:c.523A>G ENSP00000360266.2:p.Asn175Asp
NM_002228.3:c.523A>G NP_002219.1:p.Asn175Asp
NM_002228.4:c.523A>G MANE Select NP_002219.1:p.Asn175Asp
Search 100 bp 5'
Search 100 bp 3'