Canonical Allele Identifier: CA340578189
Gene: JUN HGNC NCBI

Linked Data

gnomAD v4: 1-58782569-G-A
MyVariant Identifiers: chr1:g.59248241G>A (hg19) chr1:g.58782569G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58782569G>A , CM000663.2:g.58782569G>A GRCh38
NC_000001.10:g.59248241G>A , CM000663.1:g.59248241G>A GRCh37
NC_000001.9:g.59020829G>A NCBI36
NG_047027.1:g.6545C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000710273.1:c.568C>T ENSP00000518166.1:p.Pro190Ser
ENST00000371222.4:c.502C>T MANE Select ENSP00000360266.2:p.Pro168Ser
ENST00000678696.1:c.502C>T ENSP00000503132.1:p.Pro168Ser
ENST00000371222.3:c.502C>T ENSP00000360266.2:p.Pro168Ser
NM_002228.3:c.502C>T NP_002219.1:p.Pro168Ser
NM_002228.4:c.502C>T MANE Select NP_002219.1:p.Pro168Ser
Search 100 bp 5'
Search 100 bp 3'