Canonical Allele Identifier: CA23248773

Gene: JUN

Linked Data

• dbSNP Id: rs747602628
• MyVariant Identifiers: chr1:g.59248391G>C (hg19) ; chr1:g.58782719G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58782719G>C , CM000663.2:g.58782719G>C	GRCh38
NC_000001.10:g.59248391G>C , CM000663.1:g.59248391G>C	GRCh37
NC_000001.9:g.59020979G>C	NCBI36
NG_047027.1:g.6395C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710273.1:c.418C>G	ENSP00000518166.1:p.Leu140Val
ENST00000371222.4:c.352C>G MANE Select	ENSP00000360266.2:p.Leu118Val
ENST00000678696.1:c.352C>G	ENSP00000503132.1:p.Leu118Val
ENST00000371222.3:c.352C>G	ENSP00000360266.2:p.Leu118Val
NM_002228.3:c.352C>G	NP_002219.1:p.Leu118Val
NM_002228.4:c.352C>G MANE Select	NP_002219.1:p.Leu118Val