Canonical Allele Identifier: CA878281
Gene: JUN HGNC NCBI

Linked Data

dbSNP Id: rs774939641
ExAC: 1:59248121 G / C
gnomAD v2: 1-59248121-G-C
gnomAD v3: 1-58782449-G-C
gnomAD v4: 1-58782449-G-C
MyVariant Identifiers: chr1:g.59248121G>C (hg19) chr1:g.58782449G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782449G>C , CM000663.2:g.58782449G>C GRCh38
NC_000001.10:g.59248121G>C , CM000663.1:g.59248121G>C GRCh37
NC_000001.9:g.59020709G>C NCBI36
NG_047027.1:g.6665C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.688C>G ENSP00000518166.1:p.Pro230Ala
ENST00000371222.4:c.622C>G MANE Select ENSP00000360266.2:p.Pro208Ala
ENST00000678696.1:c.622C>G ENSP00000503132.1:p.Pro208Ala
ENST00000371222.3:c.622C>G ENSP00000360266.2:p.Pro208Ala
NM_002228.3:c.622C>G NP_002219.1:p.Pro208Ala
NM_002228.4:c.622C>G MANE Select NP_002219.1:p.Pro208Ala
Search 100 bp 5'
Search 100 bp 3'