Canonical Allele Identifier: CA418188905
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs754038349
gnomAD v4: 1-58782567-C-A
MyVariant Identifiers: chr1:g.59248239C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782567C>A , CM000663.2:g.58782567C>A GRCh38
NC_000001.10:g.59248239C>A , CM000663.1:g.59248239C>A GRCh37
NC_000001.9:g.59020827C>A NCBI36
NG_047027.1:g.6547G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.570G>T ENSP00000518166.1:p.Pro190=
ENST00000371222.4:c.504G>T MANE Select ENSP00000360266.2:p.Pro168=
ENST00000678696.1:c.504G>T ENSP00000503132.1:p.Pro168=
ENST00000371222.3:c.504G>T ENSP00000360266.2:p.Pro168=
NM_002228.3:c.504G>T NP_002219.1:p.Pro168=
NM_002228.4:c.504G>T MANE Select NP_002219.1:p.Pro168=
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