Canonical Allele Identifier: CA418189038
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1296742968
gnomAD v2: 1-59248329-G-A
gnomAD v4: 1-58782657-G-A
MyVariant Identifiers: chr1:g.59248329G>A (hg19) chr1:g.58782657G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782657G>A , CM000663.2:g.58782657G>A GRCh38
NC_000001.10:g.59248329G>A , CM000663.1:g.59248329G>A GRCh37
NC_000001.9:g.59020917G>A NCBI36
NG_047027.1:g.6457C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.480C>T ENSP00000518166.1:p.Asn160=
ENST00000371222.4:c.414C>T MANE Select ENSP00000360266.2:p.Asn138=
ENST00000678696.1:c.414C>T ENSP00000503132.1:p.Asn138=
ENST00000371222.3:c.414C>T ENSP00000360266.2:p.Asn138=
NM_002228.3:c.414C>T NP_002219.1:p.Asn138=
NM_002228.4:c.414C>T MANE Select NP_002219.1:p.Asn138=
Search 100 bp 5'
Search 100 bp 3'