Canonical Allele Identifier: CA1300458869

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686613578

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325731T>C , CM000664.2:g.156325731T>C	GRCh38
NC_000002.11:g.157182243T>C , CM000664.1:g.157182243T>C	GRCh37
NC_000002.10:g.156890489T>C	NCBI36
NG_011821.1:g.12045A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*13A>G	ENSP00000514865.1:n.*13A>G
ENST00000700229.1:c.774A>G
ENST00000700230.1:c.1350A>G	ENSP00000514867.1:n.1350A>G
ENST00000700231.1:c.*13A>G	ENSP00000514868.1:n.*13A>G
ENST00000339562.9:c.*13A>G MANE Select	ENSP00000344479.4:n.*13A>G
ENST00000675870.1:c.*321A>G	ENSP00000502739.1:n.*321A>G
ENST00000339562.8:c.*13A>G	ENSP00000344479.4:n.*13A>G
ENST00000409572.5:c.*13A>G	ENSP00000386747.1:n.*13A>G
ENST00000417764.5:c.*321A>G	ENSP00000415632.1:n.*321A>G
ENST00000417972.5:c.*321A>G	ENSP00000394671.1:n.*321A>G
ENST00000426264.5:c.*13A>G	ENSP00000389986.1:n.*13A>G
NM_006186.3:c.*13A>G	NP_006177.1:n.*13A>G
XM_005246621.2:c.*13A>G	XP_005246678.1:n.*13A>G
XM_005246622.2:c.*13A>G	XP_005246679.1:n.*13A>G
XM_005246623.1:c.*13A>G	XP_005246680.1:n.*13A>G
XM_006712553.2:c.*13A>G	XP_006712616.1:n.*13A>G
XM_011511246.1:c.*44A>G	XP_011509548.1:n.*44A>G
NM_173173.2:c.*13A>G	NP_775265.1:n.*13A>G
XM_005246621.4:c.*13A>G	XP_005246678.1:n.*13A>G
XM_006712553.4:c.*13A>G	XP_006712616.1:n.*13A>G
XM_011511246.2:c.*44A>G	XP_011509548.1:n.*44A>G
XM_017004219.2:c.*13A>G	XP_016859708.1:n.*13A>G
XM_017004220.2:c.*13A>G	XP_016859709.1:n.*13A>G
XR_001738751.2:n.2057A>G
XR_001738752.2:n.1879A>G
XR_427087.4:n.1936A>G
NM_006186.4:c.*13A>G MANE Select	NP_006177.1:n.*13A>G
NM_173173.3:c.*13A>G	NP_775265.1:n.*13A>G