Canonical Allele Identifier: CA348679473

Gene: NR4A2

Linked Data

• dbSNP Id: rs1211501450
• gnomAD v3: 2-156325840-T-A
• gnomAD v4: 2-156325840-T-A
• MyVariant Identifiers: chr2:g.157182352T>A (hg19) ; chr2:g.156325840T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325840T>A , CM000664.2:g.156325840T>A	GRCh38
NC_000002.11:g.157182352T>A , CM000664.1:g.157182352T>A	GRCh37
NC_000002.10:g.156890598T>A	NCBI36
NG_011821.1:g.11936A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1497A>T	ENSP00000514865.1:p.Thr499=
ENST00000700229.1:c.665A>T
ENST00000700230.1:c.1241A>T	ENSP00000514867.1:n.1241A>T
ENST00000700231.1:c.1626A>T	ENSP00000514868.1:p.Thr542=
ENST00000339562.9:c.1701A>T MANE Select	ENSP00000344479.4:p.Thr567=
ENST00000675870.1:c.*212A>T	ENSP00000502739.1:n.*212A>T
ENST00000339562.8:c.1701A>T	ENSP00000344479.4:p.Thr567=
ENST00000409108.6:c.1597A>T	ENSP00000386993.2:p.Thr533Ser
ENST00000409572.5:c.1701A>T	ENSP00000386747.1:p.Thr567=
ENST00000417764.5:c.*212A>T	ENSP00000415632.1:n.*212A>T
ENST00000417972.5:c.*212A>T	ENSP00000394671.1:n.*212A>T
ENST00000426264.5:c.1512A>T	ENSP00000389986.1:p.Thr504=
ENST00000429376.5:c.1408A>T	ENSP00000410952.1:p.Thr470Ser
NM_006186.3:c.1701A>T	NP_006177.1:p.Thr567=
XM_005246621.2:c.1734A>T	XP_005246678.1:p.Thr578=
XM_005246622.2:c.1512A>T	XP_005246679.1:p.Thr504=
XM_005246623.1:c.1512A>T	XP_005246680.1:p.Thr504=
XM_006712553.2:c.1659A>T	XP_006712616.1:p.Thr553=
XM_011511246.1:c.1630A>T	XP_011509548.1:p.Thr544Ser
NM_173173.2:c.1512A>T	NP_775265.1:p.Thr504=
XM_005246621.4:c.1734A>T	XP_005246678.1:p.Thr578=
XM_006712553.4:c.1659A>T	XP_006712616.1:p.Thr553=
XM_011511246.2:c.1630A>T	XP_011509548.1:p.Thr544Ser
XM_017004219.2:c.1701A>T	XP_016859708.1:p.Thr567=
XM_017004220.2:c.1626A>T	XP_016859709.1:p.Thr542=
XR_001738751.2:n.1948A>T
XR_001738752.2:n.1770A>T
XR_427087.4:n.1827A>T
NM_006186.4:c.1701A>T MANE Select	NP_006177.1:p.Thr567=
NM_173173.3:c.1512A>T	NP_775265.1:p.Thr504=