Canonical Allele Identifier: CA418188715
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1207736472
gnomAD v2: 1-59248401-G-A
gnomAD v4: 1-58782729-G-A
MyVariant Identifiers: chr1:g.59248401G>A (hg19) chr1:g.58782729G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782729G>A , CM000663.2:g.58782729G>A GRCh38
NC_000001.10:g.59248401G>A , CM000663.1:g.59248401G>A GRCh37
NC_000001.9:g.59020989G>A NCBI36
NG_047027.1:g.6385C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.408C>T ENSP00000518166.1:p.Phe136=
ENST00000371222.4:c.342C>T MANE Select ENSP00000360266.2:p.Phe114=
ENST00000678696.1:c.342C>T ENSP00000503132.1:p.Phe114=
ENST00000371222.3:c.342C>T ENSP00000360266.2:p.Phe114=
NM_002228.3:c.342C>T NP_002219.1:p.Phe114=
NM_002228.4:c.342C>T MANE Select NP_002219.1:p.Phe114=
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