Canonical Allele Identifier: CA340577929
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248117T>C (hg19) chr1:g.58782445T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782445T>C , CM000663.2:g.58782445T>C GRCh38
NC_000001.10:g.59248117T>C , CM000663.1:g.59248117T>C GRCh37
NC_000001.9:g.59020705T>C NCBI36
NG_047027.1:g.6669A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.692A>G ENSP00000518166.1:p.His231Arg
ENST00000371222.4:c.626A>G MANE Select ENSP00000360266.2:p.His209Arg
ENST00000678696.1:c.626A>G ENSP00000503132.1:p.His209Arg
ENST00000371222.3:c.626A>G ENSP00000360266.2:p.His209Arg
NM_002228.3:c.626A>G NP_002219.1:p.His209Arg
NM_002228.4:c.626A>G MANE Select NP_002219.1:p.His209Arg
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