Canonical Allele Identifier: CA340578180
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1471498107
MyVariant Identifiers: chr1:g.59248237A>C (hg19) chr1:g.58782565A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782565A>C , CM000663.2:g.58782565A>C GRCh38
NC_000001.10:g.59248237A>C , CM000663.1:g.59248237A>C GRCh37
NC_000001.9:g.59020825A>C NCBI36
NG_047027.1:g.6549T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.572T>G ENSP00000518166.1:p.Val191Gly
ENST00000371222.4:c.506T>G MANE Select ENSP00000360266.2:p.Val169Gly
ENST00000678696.1:c.506T>G ENSP00000503132.1:p.Val169Gly
ENST00000371222.3:c.506T>G ENSP00000360266.2:p.Val169Gly
NM_002228.3:c.506T>G NP_002219.1:p.Val169Gly
NM_002228.4:c.506T>G MANE Select NP_002219.1:p.Val169Gly
Search 100 bp 5'
Search 100 bp 3'