Canonical Allele Identifier: CA340578086
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs2100739239
gnomAD v4: 1-58782521-C-T
MyVariant Identifiers: chr1:g.59248193C>T (hg19) chr1:g.58782521C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782521C>T , CM000663.2:g.58782521C>T GRCh38
NC_000001.10:g.59248193C>T , CM000663.1:g.59248193C>T GRCh37
NC_000001.9:g.59020781C>T NCBI36
NG_047027.1:g.6593G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.616G>A ENSP00000518166.1:p.Gly206Ser
ENST00000371222.4:c.550G>A MANE Select ENSP00000360266.2:p.Gly184Ser
ENST00000678696.1:c.550G>A ENSP00000503132.1:p.Gly184Ser
ENST00000371222.3:c.550G>A ENSP00000360266.2:p.Gly184Ser
NM_002228.3:c.550G>A NP_002219.1:p.Gly184Ser
NM_002228.4:c.550G>A MANE Select NP_002219.1:p.Gly184Ser
Search 100 bp 5'
Search 100 bp 3'