Canonical Allele Identifier: CA1300458830

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686608123

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325658C>A , CM000664.2:g.156325658C>A	GRCh38
NC_000002.11:g.157182170C>A , CM000664.1:g.157182170C>A	GRCh37
NC_000002.10:g.156890416C>A	NCBI36
NG_011821.1:g.12118G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*86G>T	ENSP00000514865.1:n.*86G>T
ENST00000700229.1:c.847G>T
ENST00000700230.1:c.1423G>T	ENSP00000514867.1:n.1423G>T
ENST00000700231.1:c.*86G>T	ENSP00000514868.1:n.*86G>T
ENST00000339562.9:c.*86G>T MANE Select	ENSP00000344479.4:n.*86G>T
ENST00000675870.1:c.*394G>T	ENSP00000502739.1:n.*394G>T
ENST00000339562.8:c.*86G>T	ENSP00000344479.4:n.*86G>T
ENST00000409572.5:c.*86G>T	ENSP00000386747.1:n.*86G>T
ENST00000417764.5:c.*394G>T	ENSP00000415632.1:n.*394G>T
ENST00000417972.5:c.*394G>T	ENSP00000394671.1:n.*394G>T
ENST00000426264.5:c.*86G>T	ENSP00000389986.1:n.*86G>T
NM_006186.3:c.*86G>T	NP_006177.1:n.*86G>T
XM_005246621.2:c.*86G>T	XP_005246678.1:n.*86G>T
XM_005246622.2:c.*86G>T	XP_005246679.1:n.*86G>T
XM_005246623.1:c.*86G>T	XP_005246680.1:n.*86G>T
XM_006712553.2:c.*86G>T	XP_006712616.1:n.*86G>T
XM_011511246.1:c.*117G>T	XP_011509548.1:n.*117G>T
NM_173173.2:c.*86G>T	NP_775265.1:n.*86G>T
XM_005246621.4:c.*86G>T	XP_005246678.1:n.*86G>T
XM_006712553.4:c.*86G>T	XP_006712616.1:n.*86G>T
XM_011511246.2:c.*117G>T	XP_011509548.1:n.*117G>T
XM_017004219.2:c.*86G>T	XP_016859708.1:n.*86G>T
XM_017004220.2:c.*86G>T	XP_016859709.1:n.*86G>T
XR_001738751.2:n.2130G>T
XR_001738752.2:n.1952G>T
XR_427087.4:n.2009G>T
NM_006186.4:c.*86G>T MANE Select	NP_006177.1:n.*86G>T
NM_173173.3:c.*86G>T	NP_775265.1:n.*86G>T