Canonical Allele Identifier: CA418188865
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739276
MyVariant Identifiers: chr1:g.59248215G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782543G>A , CM000663.2:g.58782543G>A GRCh38
NC_000001.10:g.59248215G>A , CM000663.1:g.59248215G>A GRCh37
NC_000001.9:g.59020803G>A NCBI36
NG_047027.1:g.6571C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.594C>T ENSP00000518166.1:p.Phe198=
ENST00000371222.4:c.528C>T MANE Select ENSP00000360266.2:p.Phe176=
ENST00000678696.1:c.528C>T ENSP00000503132.1:p.Phe176=
ENST00000371222.3:c.528C>T ENSP00000360266.2:p.Phe176=
NM_002228.3:c.528C>T NP_002219.1:p.Phe176=
NM_002228.4:c.528C>T MANE Select NP_002219.1:p.Phe176=
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