Canonical Allele Identifier: CA418188645

Gene: JUN

Linked Data

• dbSNP Id: rs2100738917
• MyVariant Identifiers: chr1:g.59248026T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58782354T>A , CM000663.2:g.58782354T>A	GRCh38
NC_000001.10:g.59248026T>A , CM000663.1:g.59248026T>A	GRCh37
NC_000001.9:g.59020614T>A	NCBI36
NG_047027.1:g.6760A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710273.1:c.783A>T	ENSP00000518166.1:p.Thr261=
ENST00000371222.4:c.717A>T MANE Select	ENSP00000360266.2:p.Thr239=
ENST00000678696.1:c.717A>T	ENSP00000503132.1:p.Thr239=
ENST00000371222.3:c.717A>T	ENSP00000360266.2:p.Thr239=
NM_002228.3:c.717A>T	NP_002219.1:p.Thr239=
NM_002228.4:c.717A>T MANE Select	NP_002219.1:p.Thr239=