Canonical Allele Identifier: CA340578127
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1569897293
MyVariant Identifiers: chr1:g.59248213T>G (hg19) chr1:g.58782541T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782541T>G , CM000663.2:g.58782541T>G GRCh38
NC_000001.10:g.59248213T>G , CM000663.1:g.59248213T>G GRCh37
NC_000001.9:g.59020801T>G NCBI36
NG_047027.1:g.6573A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.596A>C ENSP00000518166.1:p.Asn199Thr
ENST00000371222.4:c.530A>C MANE Select ENSP00000360266.2:p.Asn177Thr
ENST00000678696.1:c.530A>C ENSP00000503132.1:p.Asn177Thr
ENST00000371222.3:c.530A>C ENSP00000360266.2:p.Asn177Thr
NM_002228.3:c.530A>C NP_002219.1:p.Asn177Thr
NM_002228.4:c.530A>C MANE Select NP_002219.1:p.Asn177Thr
Search 100 bp 5'
Search 100 bp 3'