Canonical Allele Identifier: CA878283
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs748534142
ExAC: 1:59248123 GGCT / G
gnomAD v2: 1-59248123-GGCT-G
gnomAD v3: 1-58782451-GGCT-G
gnomAD v4: 1-58782451-GGCT-G
MyVariant Identifiers: chr1:g.59248127_59248129del (hg19) chr1:g.59248124_59248126del (hg19) chr1:g.58782455_58782457del (hg38) chr1:g.58782452_58782454del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782465_58782467del , CM000663.2:g.58782465_58782467del GRCh38
NC_000001.10:g.59248137_59248139del , CM000663.1:g.59248137_59248139del GRCh37
NC_000001.9:g.59020725_59020727del NCBI36
NG_047027.1:g.6660_6662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.683_685del ENSP00000518166.1:p.Gln228del
ENST00000371222.4:c.617_619del MANE Select ENSP00000360266.2:p.Gln206del
ENST00000678696.1:c.617_619del ENSP00000503132.1:p.Gln206del
ENST00000371222.3:c.617_619del ENSP00000360266.2:p.Gln206del
NM_002228.3:c.617_619del NP_002219.1:p.Gln206del
NM_002228.4:c.617_619del MANE Select NP_002219.1:p.Gln206del
Search 100 bp 5'
Search 100 bp 3'