Canonical Allele Identifier: CA340578366
Gene: JUN HGNC NCBI

Linked Data

gnomAD v4: 1-58782655-C-G
MyVariant Identifiers: chr1:g.59248327C>G (hg19) chr1:g.58782655C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782655C>G , CM000663.2:g.58782655C>G GRCh38
NC_000001.10:g.59248327C>G , CM000663.1:g.59248327C>G GRCh37
NC_000001.9:g.59020915C>G NCBI36
NG_047027.1:g.6459G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.482G>C ENSP00000518166.1:p.Gly161Ala
ENST00000371222.4:c.416G>C MANE Select ENSP00000360266.2:p.Gly139Ala
ENST00000678696.1:c.416G>C ENSP00000503132.1:p.Gly139Ala
ENST00000371222.3:c.416G>C ENSP00000360266.2:p.Gly139Ala
NM_002228.3:c.416G>C NP_002219.1:p.Gly139Ala
NM_002228.4:c.416G>C MANE Select NP_002219.1:p.Gly139Ala
Search 100 bp 5'
Search 100 bp 3'