Canonical Allele Identifier: CA418188853
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1645584462
gnomAD v4: 1-58782537-T-G
MyVariant Identifiers: chr1:g.59248209T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782537T>G , CM000663.2:g.58782537T>G GRCh38
NC_000001.10:g.59248209T>G , CM000663.1:g.59248209T>G GRCh37
NC_000001.9:g.59020797T>G NCBI36
NG_047027.1:g.6577A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.600A>C ENSP00000518166.1:p.Pro200=
ENST00000371222.4:c.534A>C MANE Select ENSP00000360266.2:p.Pro178=
ENST00000678696.1:c.534A>C ENSP00000503132.1:p.Pro178=
ENST00000371222.3:c.534A>C ENSP00000360266.2:p.Pro178=
NM_002228.3:c.534A>C NP_002219.1:p.Pro178=
NM_002228.4:c.534A>C MANE Select NP_002219.1:p.Pro178=
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