Canonical Allele Identifier: CA878261
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs776063293
ExAC: 1:59247997 G / A
gnomAD v2: 1-59247997-G-A
gnomAD v4: 1-58782325-G-A
MyVariant Identifiers: chr1:g.59247997G>A (hg19) chr1:g.58782325G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782325G>A , CM000663.2:g.58782325G>A GRCh38
NC_000001.10:g.59247997G>A , CM000663.1:g.59247997G>A GRCh37
NC_000001.9:g.59020585G>A NCBI36
NG_047027.1:g.6789C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000710273.1:c.812C>T ENSP00000518166.1:p.Ser271Phe
ENST00000371222.4:c.746C>T MANE Select ENSP00000360266.2:p.Ser249Phe
ENST00000678696.1:c.746C>T ENSP00000503132.1:p.Ser249Phe
ENST00000371222.3:c.746C>T ENSP00000360266.2:p.Ser249Phe
NM_002228.3:c.746C>T NP_002219.1:p.Ser249Phe
NM_002228.4:c.746C>T MANE Select NP_002219.1:p.Ser249Phe
Search 100 bp 5'
Search 100 bp 3'