Canonical Allele Identifier: CA59154782

Gene: NR4A2

Linked Data

• dbSNP Id: rs1030420744
• gnomAD v2: 2-157182337-G-T
• gnomAD v3: 2-156325825-G-T
• gnomAD v4: 2-156325825-G-T
• MyVariant Identifiers: chr2:g.157182337G>T (hg19) ; chr2:g.156325825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325825G>T , CM000664.2:g.156325825G>T	GRCh38
NC_000002.11:g.157182337G>T , CM000664.1:g.157182337G>T	GRCh37
NC_000002.10:g.156890583G>T	NCBI36
NG_011821.1:g.11951C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1512C>A	ENSP00000514865.1:p.Arg504=
ENST00000700229.1:c.680C>A
ENST00000700230.1:c.1256C>A	ENSP00000514867.1:n.1256C>A
ENST00000700231.1:c.1641C>A	ENSP00000514868.1:p.Arg547=
ENST00000339562.9:c.1716C>A MANE Select	ENSP00000344479.4:p.Arg572=
ENST00000675870.1:c.*227C>A	ENSP00000502739.1:n.*227C>A
ENST00000339562.8:c.1716C>A	ENSP00000344479.4:p.Arg572=
ENST00000409108.6:c.1612C>A	ENSP00000386993.2:p.His538Asn
ENST00000409572.5:c.1716C>A	ENSP00000386747.1:p.Arg572=
ENST00000417764.5:c.*227C>A	ENSP00000415632.1:n.*227C>A
ENST00000417972.5:c.*227C>A	ENSP00000394671.1:n.*227C>A
ENST00000426264.5:c.1527C>A	ENSP00000389986.1:p.Arg509=
ENST00000429376.5:c.1423C>A	ENSP00000410952.1:p.His475Asn
NM_006186.3:c.1716C>A	NP_006177.1:p.Arg572=
XM_005246621.2:c.1749C>A	XP_005246678.1:p.Arg583=
XM_005246622.2:c.1527C>A	XP_005246679.1:p.Arg509=
XM_005246623.1:c.1527C>A	XP_005246680.1:p.Arg509=
XM_006712553.2:c.1674C>A	XP_006712616.1:p.Arg558=
XM_011511246.1:c.1645C>A	XP_011509548.1:p.His549Asn
NM_173173.2:c.1527C>A	NP_775265.1:p.Arg509=
XM_005246621.4:c.1749C>A	XP_005246678.1:p.Arg583=
XM_006712553.4:c.1674C>A	XP_006712616.1:p.Arg558=
XM_011511246.2:c.1645C>A	XP_011509548.1:p.His549Asn
XM_017004219.2:c.1716C>A	XP_016859708.1:p.Arg572=
XM_017004220.2:c.1641C>A	XP_016859709.1:p.Arg547=
XR_001738751.2:n.1963C>A
XR_001738752.2:n.1785C>A
XR_427087.4:n.1842C>A
NM_006186.4:c.1716C>A MANE Select	NP_006177.1:p.Arg572=
NM_173173.3:c.1527C>A	NP_775265.1:p.Arg509=