Canonical Allele Identifier: CA418188911
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1377912249
MyVariant Identifiers: chr1:g.59248242C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782570C>G , CM000663.2:g.58782570C>G GRCh38
NC_000001.10:g.59248242C>G , CM000663.1:g.59248242C>G GRCh37
NC_000001.9:g.59020830C>G NCBI36
NG_047027.1:g.6544G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.567G>C ENSP00000518166.1:p.Pro189=
ENST00000371222.4:c.501G>C MANE Select ENSP00000360266.2:p.Pro167=
ENST00000678696.1:c.501G>C ENSP00000503132.1:p.Pro167=
ENST00000371222.3:c.501G>C ENSP00000360266.2:p.Pro167=
NM_002228.3:c.501G>C NP_002219.1:p.Pro167=
NM_002228.4:c.501G>C MANE Select NP_002219.1:p.Pro167=
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