Canonical Allele Identifier: CA418188969
Gene: JUN HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59248284G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782612G>C , CM000663.2:g.58782612G>C GRCh38
NC_000001.10:g.59248284G>C , CM000663.1:g.59248284G>C GRCh37
NC_000001.9:g.59020872G>C NCBI36
NG_047027.1:g.6502C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.525C>G ENSP00000518166.1:p.Gly175=
ENST00000371222.4:c.459C>G MANE Select ENSP00000360266.2:p.Gly153=
ENST00000678696.1:c.459C>G ENSP00000503132.1:p.Gly153=
ENST00000371222.3:c.459C>G ENSP00000360266.2:p.Gly153=
NM_002228.3:c.459C>G NP_002219.1:p.Gly153=
NM_002228.4:c.459C>G MANE Select NP_002219.1:p.Gly153=
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