Canonical Allele Identifier: CA418188922
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248254C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782582C>A , CM000663.2:g.58782582C>A GRCh38
NC_000001.10:g.59248254C>A , CM000663.1:g.59248254C>A GRCh37
NC_000001.9:g.59020842C>A NCBI36
NG_047027.1:g.6532G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.555G>T ENSP00000518166.1:p.Leu185=
ENST00000371222.4:c.489G>T MANE Select ENSP00000360266.2:p.Leu163=
ENST00000678696.1:c.489G>T ENSP00000503132.1:p.Leu163=
ENST00000371222.3:c.489G>T ENSP00000360266.2:p.Leu163=
NM_002228.3:c.489G>T NP_002219.1:p.Leu163=
NM_002228.4:c.489G>T MANE Select NP_002219.1:p.Leu163=
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Search 100 bp 3'