Canonical Allele Identifier: CA429727972

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686818933
• MyVariant Identifiers: chr2:g.157186087C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329575C>T , CM000664.2:g.156329575C>T	GRCh38
NC_000002.11:g.157186087C>T , CM000664.1:g.157186087C>T	GRCh37
NC_000002.10:g.156894333C>T	NCBI36
NG_011821.1:g.8201G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.423G>A	ENSP00000388120.2:p.Pro141=
ENST00000700228.1:c.483G>A	ENSP00000514865.1:p.Pro161=
ENST00000700230.1:c.45G>A	ENSP00000514867.1:p.Pro15=
ENST00000700231.1:c.612G>A	ENSP00000514868.1:p.Pro204=
ENST00000339562.9:c.612G>A MANE Select	ENSP00000344479.4:p.Pro204=
ENST00000675870.1:c.423G>A	ENSP00000502739.1:p.Pro141=
ENST00000339562.8:c.612G>A	ENSP00000344479.4:p.Pro204=
ENST00000406048.2:c.208+339G>A
ENST00000409108.6:c.612G>A	ENSP00000386993.2:p.Pro204=
ENST00000409572.5:c.612G>A	ENSP00000386747.1:p.Pro204=
ENST00000417764.5:c.423G>A	ENSP00000415632.1:p.Pro141=
ENST00000417972.5:c.423G>A	ENSP00000394671.1:p.Pro141=
ENST00000424077.1:c.612G>A	ENSP00000406808.1:p.Pro204=
ENST00000426264.5:c.423G>A	ENSP00000389986.1:p.Pro141=
ENST00000429376.5:c.423G>A	ENSP00000410952.1:p.Pro141=
NM_006186.3:c.612G>A	NP_006177.1:p.Pro204=
XM_005246621.2:c.645G>A	XP_005246678.1:p.Pro215=
XM_005246622.2:c.423G>A	XP_005246679.1:p.Pro141=
XM_005246623.1:c.423G>A	XP_005246680.1:p.Pro141=
XM_006712553.2:c.645G>A	XP_006712616.1:p.Pro215=
XM_011511246.1:c.645G>A	XP_011509548.1:p.Pro215=
XR_427087.2:n.2818G>A
NM_173173.2:c.423G>A	NP_775265.1:p.Pro141=
XM_005246621.4:c.645G>A	XP_005246678.1:p.Pro215=
XM_006712553.4:c.645G>A	XP_006712616.1:p.Pro215=
XM_011511246.2:c.645G>A	XP_011509548.1:p.Pro215=
XM_017004219.2:c.612G>A	XP_016859708.1:p.Pro204=
XM_017004220.2:c.612G>A	XP_016859709.1:p.Pro204=
XR_001738751.2:n.980G>A
XR_001738752.2:n.802G>A
XR_427087.4:n.859G>A
NM_006186.4:c.612G>A MANE Select	NP_006177.1:p.Pro204=
NM_173173.3:c.423G>A	NP_775265.1:p.Pro141=