Canonical Allele Identifier: CA1916206

Gene: NR4A2

Linked Data

• dbSNP Id: rs757815729
• ExAC: 2:157182687 G / A
• gnomAD v2: 2-157182687-G-A
• gnomAD v3: 2-156326175-G-A
• gnomAD v4: 2-156326175-G-A
• MyVariant Identifiers: chr2:g.157182687G>A (hg19) ; chr2:g.156326175G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326175G>A , CM000664.2:g.156326175G>A	GRCh38
NC_000002.11:g.157182687G>A , CM000664.1:g.157182687G>A	GRCh37
NC_000002.10:g.156890933G>A	NCBI36
NG_011821.1:g.11601C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1311C>T	ENSP00000514865.1:p.Cys437=
ENST00000700229.1:c.479C>T
ENST00000700230.1:c.1055C>T	ENSP00000514867.1:n.1055C>T
ENST00000700231.1:c.1440C>T	ENSP00000514868.1:p.Cys480=
ENST00000339562.9:c.1515C>T MANE Select	ENSP00000344479.4:p.Cys505=
ENST00000675870.1:c.*26C>T	ENSP00000502739.1:n.*26C>T
ENST00000339562.8:c.1515C>T	ENSP00000344479.4:p.Cys505=
ENST00000409108.6:c.1411C>T	ENSP00000386993.2:p.His471Tyr
ENST00000409572.5:c.1515C>T	ENSP00000386747.1:p.Cys505=
ENST00000417764.5:c.*26C>T	ENSP00000415632.1:n.*26C>T
ENST00000417972.5:c.*26C>T	ENSP00000394671.1:n.*26C>T
ENST00000426264.5:c.1326C>T	ENSP00000389986.1:p.Cys442=
ENST00000429376.5:c.1222C>T	ENSP00000410952.1:p.His408Tyr
NM_006186.3:c.1515C>T	NP_006177.1:p.Cys505=
XM_005246621.2:c.1548C>T	XP_005246678.1:p.Cys516=
XM_005246622.2:c.1326C>T	XP_005246679.1:p.Cys442=
XM_005246623.1:c.1326C>T	XP_005246680.1:p.Cys442=
XM_006712553.2:c.1473C>T	XP_006712616.1:p.Cys491=
XM_011511246.1:c.1444C>T	XP_011509548.1:p.His482Tyr
XR_427087.2:n.3600C>T
NM_173173.2:c.1326C>T	NP_775265.1:p.Cys442=
XM_005246621.4:c.1548C>T	XP_005246678.1:p.Cys516=
XM_006712553.4:c.1473C>T	XP_006712616.1:p.Cys491=
XM_011511246.2:c.1444C>T	XP_011509548.1:p.His482Tyr
XM_017004219.2:c.1515C>T	XP_016859708.1:p.Cys505=
XM_017004220.2:c.1440C>T	XP_016859709.1:p.Cys480=
XR_001738751.2:n.1762C>T
XR_001738752.2:n.1584C>T
XR_427087.4:n.1641C>T
NM_006186.4:c.1515C>T MANE Select	NP_006177.1:p.Cys505=
NM_173173.3:c.1326C>T	NP_775265.1:p.Cys442=