Canonical Allele Identifier: CA429727779
Gene: NR4A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.157185973C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329461C>T , CM000664.2:g.156329461C>T GRCh38
NC_000002.11:g.157185973C>T , CM000664.1:g.157185973C>T GRCh37
NC_000002.10:g.156894219C>T NCBI36
NG_011821.1:g.8315G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700228.1:c.597G>A ENSP00000514865.1:p.Gln199=
ENST00000700230.1:c.159G>A ENSP00000514867.1:p.Gln53=
ENST00000700231.1:c.726G>A ENSP00000514868.1:p.Gln242=
ENST00000339562.9:c.726G>A MANE Select ENSP00000344479.4:p.Gln242=
ENST00000675870.1:c.537G>A ENSP00000502739.1:p.Gln179=
ENST00000339562.8:c.726G>A ENSP00000344479.4:p.Gln242=
ENST00000406048.2:c.208+453G>A
ENST00000409108.6:c.726G>A ENSP00000386993.2:p.Gln242=
ENST00000409572.5:c.726G>A ENSP00000386747.1:p.Gln242=
ENST00000417764.5:c.537G>A ENSP00000415632.1:p.Gln179=
ENST00000417972.5:c.537G>A ENSP00000394671.1:p.Gln179=
ENST00000424077.1:c.726G>A ENSP00000406808.1:p.Gln242=
ENST00000426264.5:c.537G>A ENSP00000389986.1:p.Gln179=
ENST00000429376.5:c.537G>A ENSP00000410952.1:p.Gln179=
NM_006186.3:c.726G>A NP_006177.1:p.Gln242=
XM_005246621.2:c.759G>A XP_005246678.1:p.Gln253=
XM_005246622.2:c.537G>A XP_005246679.1:p.Gln179=
XM_005246623.1:c.537G>A XP_005246680.1:p.Gln179=
XM_006712553.2:c.759G>A XP_006712616.1:p.Gln253=
XM_011511246.1:c.759G>A XP_011509548.1:p.Gln253=
XR_427087.2:n.2932G>A
NM_173173.2:c.537G>A NP_775265.1:p.Gln179=
XM_005246621.4:c.759G>A XP_005246678.1:p.Gln253=
XM_006712553.4:c.759G>A XP_006712616.1:p.Gln253=
XM_011511246.2:c.759G>A XP_011509548.1:p.Gln253=
XM_017004219.2:c.726G>A XP_016859708.1:p.Gln242=
XM_017004220.2:c.726G>A XP_016859709.1:p.Gln242=
XR_001738751.2:n.1094G>A
XR_001738752.2:n.916G>A
XR_427087.4:n.973G>A
NM_006186.4:c.726G>A MANE Select NP_006177.1:p.Gln242=
NM_173173.3:c.537G>A NP_775265.1:p.Gln179=