Canonical Allele Identifier: CA340577931
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1241847047
gnomAD v4: 1-58782446-G-A
MyVariant Identifiers: chr1:g.59248118G>A (hg19) chr1:g.58782446G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782446G>A , CM000663.2:g.58782446G>A GRCh38
NC_000001.10:g.59248118G>A , CM000663.1:g.59248118G>A GRCh37
NC_000001.9:g.59020706G>A NCBI36
NG_047027.1:g.6668C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.691C>T ENSP00000518166.1:p.His231Tyr
ENST00000371222.4:c.625C>T MANE Select ENSP00000360266.2:p.His209Tyr
ENST00000678696.1:c.625C>T ENSP00000503132.1:p.His209Tyr
ENST00000371222.3:c.625C>T ENSP00000360266.2:p.His209Tyr
NM_002228.3:c.625C>T NP_002219.1:p.His209Tyr
NM_002228.4:c.625C>T MANE Select NP_002219.1:p.His209Tyr
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