Canonical Allele Identifier: CA348679961

Gene: NR4A2

Linked Data

• dbSNP Id: rs1371554953
• gnomAD v2: 2-157182674-C-T
• gnomAD v4: 2-156326162-C-T
• MyVariant Identifiers: chr2:g.157182674C>T (hg19) ; chr2:g.156326162C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326162C>T , CM000664.2:g.156326162C>T	GRCh38
NC_000002.11:g.157182674C>T , CM000664.1:g.157182674C>T	GRCh37
NC_000002.10:g.156890920C>T	NCBI36
NG_011821.1:g.11614G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1324G>A	ENSP00000514865.1:p.Ala442Thr
ENST00000700229.1:c.492G>A
ENST00000700230.1:c.1068G>A	ENSP00000514867.1:n.1068G>A
ENST00000700231.1:c.1453G>A	ENSP00000514868.1:p.Ala485Thr
ENST00000339562.9:c.1528G>A MANE Select	ENSP00000344479.4:p.Ala510Thr
ENST00000675870.1:c.*39G>A	ENSP00000502739.1:n.*39G>A
ENST00000339562.8:c.1528G>A	ENSP00000344479.4:p.Ala510Thr
ENST00000409108.6:c.1424G>A	ENSP00000386993.2:p.Gly475Asp
ENST00000409572.5:c.1528G>A	ENSP00000386747.1:p.Ala510Thr
ENST00000417764.5:c.*39G>A	ENSP00000415632.1:n.*39G>A
ENST00000417972.5:c.*39G>A	ENSP00000394671.1:n.*39G>A
ENST00000426264.5:c.1339G>A	ENSP00000389986.1:p.Ala447Thr
ENST00000429376.5:c.1235G>A	ENSP00000410952.1:p.Gly412Asp
NM_006186.3:c.1528G>A	NP_006177.1:p.Ala510Thr
XM_005246621.2:c.1561G>A	XP_005246678.1:p.Ala521Thr
XM_005246622.2:c.1339G>A	XP_005246679.1:p.Ala447Thr
XM_005246623.1:c.1339G>A	XP_005246680.1:p.Ala447Thr
XM_006712553.2:c.1486G>A	XP_006712616.1:p.Ala496Thr
XM_011511246.1:c.1457G>A	XP_011509548.1:p.Gly486Asp
XR_427087.2:n.3613G>A
NM_173173.2:c.1339G>A	NP_775265.1:p.Ala447Thr
XM_005246621.4:c.1561G>A	XP_005246678.1:p.Ala521Thr
XM_006712553.4:c.1486G>A	XP_006712616.1:p.Ala496Thr
XM_011511246.2:c.1457G>A	XP_011509548.1:p.Gly486Asp
XM_017004219.2:c.1528G>A	XP_016859708.1:p.Ala510Thr
XM_017004220.2:c.1453G>A	XP_016859709.1:p.Ala485Thr
XR_001738751.2:n.1775G>A
XR_001738752.2:n.1597G>A
XR_427087.4:n.1654G>A
NM_006186.4:c.1528G>A MANE Select	NP_006177.1:p.Ala510Thr
NM_173173.3:c.1339G>A	NP_775265.1:p.Ala447Thr