Canonical Allele Identifier: CA59154779

Gene: NR4A2

Linked Data

• dbSNP Id: rs182677667
• gnomAD v3: 2-156325680-A-G
• gnomAD v4: 2-156325680-A-G
• MyVariant Identifiers: chr2:g.157182192A>G (hg19) ; chr2:g.156325680A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325680A>G , CM000664.2:g.156325680A>G	GRCh38
NC_000002.11:g.157182192A>G , CM000664.1:g.157182192A>G	GRCh37
NC_000002.10:g.156890438A>G	NCBI36
NG_011821.1:g.12096T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*64T>C	ENSP00000514865.1:n.*64T>C
ENST00000700229.1:c.825T>C
ENST00000700230.1:c.1401T>C	ENSP00000514867.1:n.1401T>C
ENST00000700231.1:c.*64T>C	ENSP00000514868.1:n.*64T>C
ENST00000339562.9:c.*64T>C MANE Select	ENSP00000344479.4:n.*64T>C
ENST00000675870.1:c.*372T>C	ENSP00000502739.1:n.*372T>C
ENST00000339562.8:c.*64T>C	ENSP00000344479.4:n.*64T>C
ENST00000409572.5:c.*64T>C	ENSP00000386747.1:n.*64T>C
ENST00000417764.5:c.*372T>C	ENSP00000415632.1:n.*372T>C
ENST00000417972.5:c.*372T>C	ENSP00000394671.1:n.*372T>C
ENST00000426264.5:c.*64T>C	ENSP00000389986.1:n.*64T>C
NM_006186.3:c.*64T>C	NP_006177.1:n.*64T>C
XM_005246621.2:c.*64T>C	XP_005246678.1:n.*64T>C
XM_005246622.2:c.*64T>C	XP_005246679.1:n.*64T>C
XM_005246623.1:c.*64T>C	XP_005246680.1:n.*64T>C
XM_006712553.2:c.*64T>C	XP_006712616.1:n.*64T>C
XM_011511246.1:c.*95T>C	XP_011509548.1:n.*95T>C
NM_173173.2:c.*64T>C	NP_775265.1:n.*64T>C
XM_005246621.4:c.*64T>C	XP_005246678.1:n.*64T>C
XM_006712553.4:c.*64T>C	XP_006712616.1:n.*64T>C
XM_011511246.2:c.*95T>C	XP_011509548.1:n.*95T>C
XM_017004219.2:c.*64T>C	XP_016859708.1:n.*64T>C
XM_017004220.2:c.*64T>C	XP_016859709.1:n.*64T>C
XR_001738751.2:n.2108T>C
XR_001738752.2:n.1930T>C
XR_427087.4:n.1987T>C
NM_006186.4:c.*64T>C MANE Select	NP_006177.1:n.*64T>C
NM_173173.3:c.*64T>C	NP_775265.1:n.*64T>C