Canonical Allele Identifier: CA340578007
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248153A>C (hg19) chr1:g.58782481A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782481A>C , CM000663.2:g.58782481A>C GRCh38
NC_000001.10:g.59248153A>C , CM000663.1:g.59248153A>C GRCh37
NC_000001.9:g.59020741A>C NCBI36
NG_047027.1:g.6633T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.656T>G ENSP00000518166.1:p.Phe219Cys
ENST00000371222.4:c.590T>G MANE Select ENSP00000360266.2:p.Phe197Cys
ENST00000678696.1:c.590T>G ENSP00000503132.1:p.Phe197Cys
ENST00000371222.3:c.590T>G ENSP00000360266.2:p.Phe197Cys
NM_002228.3:c.590T>G NP_002219.1:p.Phe197Cys
NM_002228.4:c.590T>G MANE Select NP_002219.1:p.Phe197Cys
Search 100 bp 5'
Search 100 bp 3'