Canonical Allele Identifier: CA340578174
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782562T>A , CM000663.2:g.58782562T>A GRCh38
NC_000001.10:g.59248234T>A , CM000663.1:g.59248234T>A GRCh37
NC_000001.9:g.59020822T>A NCBI36
NG_047027.1:g.6552A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.575A>T ENSP00000518166.1:p.Tyr192Phe
ENST00000371222.4:c.509A>T MANE Select ENSP00000360266.2:p.Tyr170Phe
ENST00000678696.1:c.509A>T ENSP00000503132.1:p.Tyr170Phe
ENST00000371222.3:c.509A>T ENSP00000360266.2:p.Tyr170Phe
NM_002228.3:c.509A>T NP_002219.1:p.Tyr170Phe
NM_002228.4:c.509A>T MANE Select NP_002219.1:p.Tyr170Phe