Canonical Allele Identifier: CA878322
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs768130439
ExAC: 1:59248305 C / G
gnomAD v2: 1-59248305-C-G
gnomAD v4: 1-58782633-C-G
MyVariant Identifiers: chr1:g.59248305C>G (hg19) chr1:g.58782633C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782633C>G , CM000663.2:g.58782633C>G GRCh38
NC_000001.10:g.59248305C>G , CM000663.1:g.59248305C>G GRCh37
NC_000001.9:g.59020893C>G NCBI36
NG_047027.1:g.6481G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.504G>C ENSP00000518166.1:p.Ala168=
ENST00000371222.4:c.438G>C MANE Select ENSP00000360266.2:p.Ala146=
ENST00000678696.1:c.438G>C ENSP00000503132.1:p.Ala146=
ENST00000371222.3:c.438G>C ENSP00000360266.2:p.Ala146=
NM_002228.3:c.438G>C NP_002219.1:p.Ala146=
NM_002228.4:c.438G>C MANE Select NP_002219.1:p.Ala146=
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