Canonical Allele Identifier: CA23248753
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs908690389
gnomAD v3: 1-58782236-G-A
gnomAD v4: 1-58782236-G-A
MyVariant Identifiers: chr1:g.59247908G>A (hg19) chr1:g.58782236G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782236G>A , CM000663.2:g.58782236G>A GRCh38
NC_000001.10:g.59247908G>A , CM000663.1:g.59247908G>A GRCh37
NC_000001.9:g.59020496G>A NCBI36
NG_047027.1:g.6878C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710273.1:c.901C>T ENSP00000518166.1:p.Arg301Trp
ENST00000371222.4:c.835C>T MANE Select ENSP00000360266.2:p.Arg279Trp
ENST00000678696.1:c.835C>T ENSP00000503132.1:p.Arg279Trp
ENST00000371222.3:c.835C>T ENSP00000360266.2:p.Arg279Trp
NM_002228.3:c.835C>T NP_002219.1:p.Arg279Trp
NM_002228.4:c.835C>T MANE Select NP_002219.1:p.Arg279Trp
Search 100 bp 5'
Search 100 bp 3'