Canonical Allele Identifier: CA878311
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs766698964
ExAC: 1:59248233 G / A
gnomAD v2: 1-59248233-G-A
gnomAD v3: 1-58782561-G-A
gnomAD v4: 1-58782561-G-A
MyVariant Identifiers: chr1:g.59248233G>A (hg19) chr1:g.58782561G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782561G>A , CM000663.2:g.58782561G>A GRCh38
NC_000001.10:g.59248233G>A , CM000663.1:g.59248233G>A GRCh37
NC_000001.9:g.59020821G>A NCBI36
NG_047027.1:g.6553C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.576C>T ENSP00000518166.1:p.Tyr192=
ENST00000371222.4:c.510C>T MANE Select ENSP00000360266.2:p.Tyr170=
ENST00000678696.1:c.510C>T ENSP00000503132.1:p.Tyr170=
ENST00000371222.3:c.510C>T ENSP00000360266.2:p.Tyr170=
NM_002228.3:c.510C>T NP_002219.1:p.Tyr170=
NM_002228.4:c.510C>T MANE Select NP_002219.1:p.Tyr170=
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