Canonical Allele Identifier: CA340577932
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248118G>C (hg19) chr1:g.58782446G>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.691C>G ENSP00000518166.1:p.His231Asp
ENST00000371222.4:c.625C>G MANE Select ENSP00000360266.2:p.His209Asp
ENST00000678696.1:c.625C>G ENSP00000503132.1:p.His209Asp
ENST00000371222.3:c.625C>G ENSP00000360266.2:p.His209Asp
NM_002228.3:c.625C>G NP_002219.1:p.His209Asp
NM_002228.4:c.625C>G MANE Select NP_002219.1:p.His209Asp
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