Canonical Allele Identifier: CA348682673

Gene: NR4A2

Linked Data

• dbSNP Id: rs1487213200
• gnomAD v2: 2-157186371-A-T
• gnomAD v4: 2-156329859-A-T
• MyVariant Identifiers: chr2:g.157186371A>T (hg19) ; chr2:g.156329859A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329859A>T , CM000664.2:g.156329859A>T	GRCh38
NC_000002.11:g.157186371A>T , CM000664.1:g.157186371A>T	GRCh37
NC_000002.10:g.156894617A>T	NCBI36
NG_011821.1:g.7917T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.139T>A	ENSP00000388120.2:p.Ser47Thr
ENST00000700228.1:c.199T>A	ENSP00000514865.1:p.Ser67Thr
ENST00000700231.1:c.328T>A	ENSP00000514868.1:p.Ser110Thr
ENST00000339562.9:c.328T>A MANE Select	ENSP00000344479.4:p.Ser110Thr
ENST00000675870.1:c.139T>A	ENSP00000502739.1:p.Ser47Thr
ENST00000339562.8:c.328T>A	ENSP00000344479.4:p.Ser110Thr
ENST00000406048.2:c.208+55T>A
ENST00000409108.6:c.328T>A	ENSP00000386993.2:p.Ser110Thr
ENST00000409572.5:c.328T>A	ENSP00000386747.1:p.Ser110Thr
ENST00000417764.5:c.139T>A	ENSP00000415632.1:p.Ser47Thr
ENST00000417972.5:c.139T>A	ENSP00000394671.1:p.Ser47Thr
ENST00000421709.1:c.139T>A	ENSP00000388120.1:p.Ser47Thr
ENST00000424077.1:c.328T>A	ENSP00000406808.1:p.Ser110Thr
ENST00000426264.5:c.139T>A	ENSP00000389986.1:p.Ser47Thr
ENST00000429376.5:c.139T>A	ENSP00000410952.1:p.Ser47Thr
NM_006186.3:c.328T>A	NP_006177.1:p.Ser110Thr
XM_005246621.2:c.361T>A	XP_005246678.1:p.Ser121Thr
XM_005246622.2:c.139T>A	XP_005246679.1:p.Ser47Thr
XM_005246623.1:c.139T>A	XP_005246680.1:p.Ser47Thr
XM_006712553.2:c.361T>A	XP_006712616.1:p.Ser121Thr
XM_011511246.1:c.361T>A	XP_011509548.1:p.Ser121Thr
XR_427087.2:n.2534T>A
NM_173173.2:c.139T>A	NP_775265.1:p.Ser47Thr
XM_005246621.4:c.361T>A	XP_005246678.1:p.Ser121Thr
XM_006712553.4:c.361T>A	XP_006712616.1:p.Ser121Thr
XM_011511246.2:c.361T>A	XP_011509548.1:p.Ser121Thr
XM_017004219.2:c.328T>A	XP_016859708.1:p.Ser110Thr
XM_017004220.2:c.328T>A	XP_016859709.1:p.Ser110Thr
XR_001738751.2:n.696T>A
XR_001738752.2:n.518T>A
XR_427087.4:n.575T>A
NM_006186.4:c.328T>A MANE Select	NP_006177.1:p.Ser110Thr
NM_173173.3:c.139T>A	NP_775265.1:p.Ser47Thr