Canonical Allele Identifier: CA340578409
Gene: JUN HGNC NCBI

Linked Data

ClinVar Variation Id: 3112557
ClinVar RCV Id: RCV004403468
dbSNP Id: rs1247923524
gnomAD v2: 1-59248349-A-G
gnomAD v4: 1-58782677-A-G
MyVariant Identifiers: chr1:g.59248349A>G (hg19) chr1:g.58782677A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782677A>G , CM000663.2:g.58782677A>G GRCh38
NC_000001.10:g.59248349A>G , CM000663.1:g.59248349A>G GRCh37
NC_000001.9:g.59020937A>G NCBI36
NG_047027.1:g.6437T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.460T>C ENSP00000518166.1:p.Ser154Pro
ENST00000371222.4:c.394T>C MANE Select ENSP00000360266.2:p.Ser132Pro
ENST00000678696.1:c.394T>C ENSP00000503132.1:p.Ser132Pro
ENST00000371222.3:c.394T>C ENSP00000360266.2:p.Ser132Pro
NM_002228.3:c.394T>C NP_002219.1:p.Ser132Pro
NM_002228.4:c.394T>C MANE Select NP_002219.1:p.Ser132Pro
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