Canonical Allele Identifier: CA418188882
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs1439443778
gnomAD v2: 1-59248224-G-C
MyVariant Identifiers: chr1:g.59248224G>C (hg19) chr1:g.58782552G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782552G>C , CM000663.2:g.58782552G>C GRCh38
NC_000001.10:g.59248224G>C , CM000663.1:g.59248224G>C GRCh37
NC_000001.9:g.59020812G>C NCBI36
NG_047027.1:g.6562C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.585C>G ENSP00000518166.1:p.Leu195=
ENST00000371222.4:c.519C>G MANE Select ENSP00000360266.2:p.Leu173=
ENST00000678696.1:c.519C>G ENSP00000503132.1:p.Leu173=
ENST00000371222.3:c.519C>G ENSP00000360266.2:p.Leu173=
NM_002228.3:c.519C>G NP_002219.1:p.Leu173=
NM_002228.4:c.519C>G MANE Select NP_002219.1:p.Leu173=
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