Canonical Allele Identifier: CA418189112

Gene: JUN

Linked Data

• dbSNP Id: rs2100739653
• MyVariant Identifiers: chr1:g.59248382G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58782710G>A , CM000663.2:g.58782710G>A	GRCh38
NC_000001.10:g.59248382G>A , CM000663.1:g.59248382G>A	GRCh37
NC_000001.9:g.59020970G>A	NCBI36
NG_047027.1:g.6404C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710273.1:c.427C>T	ENSP00000518166.1:p.Leu143=
ENST00000371222.4:c.361C>T MANE Select	ENSP00000360266.2:p.Leu121=
ENST00000678696.1:c.361C>T	ENSP00000503132.1:p.Leu121=
ENST00000371222.3:c.361C>T	ENSP00000360266.2:p.Leu121=
NM_002228.3:c.361C>T	NP_002219.1:p.Leu121=
NM_002228.4:c.361C>T MANE Select	NP_002219.1:p.Leu121=