Canonical Allele Identifier: CA59154772

Gene: NR4A2

Linked Data

• dbSNP Id: rs1036732619
• gnomAD v3: 2-156325635-G-C
• gnomAD v4: 2-156325635-G-C
• MyVariant Identifiers: chr2:g.157182147G>C (hg19) ; chr2:g.156325635G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325635G>C , CM000664.2:g.156325635G>C	GRCh38
NC_000002.11:g.157182147G>C , CM000664.1:g.157182147G>C	GRCh37
NC_000002.10:g.156890393G>C	NCBI36
NG_011821.1:g.12141C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*109C>G	ENSP00000514865.1:n.*109C>G
ENST00000700229.1:c.870C>G
ENST00000700230.1:c.1446C>G	ENSP00000514867.1:n.1446C>G
ENST00000700231.1:c.*109C>G	ENSP00000514868.1:n.*109C>G
ENST00000339562.9:c.*109C>G MANE Select	ENSP00000344479.4:n.*109C>G
ENST00000675870.1:c.*417C>G	ENSP00000502739.1:n.*417C>G
ENST00000339562.8:c.*109C>G	ENSP00000344479.4:n.*109C>G
ENST00000409572.5:c.*109C>G	ENSP00000386747.1:n.*109C>G
ENST00000417764.5:c.*417C>G	ENSP00000415632.1:n.*417C>G
ENST00000417972.5:c.*417C>G	ENSP00000394671.1:n.*417C>G
ENST00000426264.5:c.*109C>G	ENSP00000389986.1:n.*109C>G
NM_006186.3:c.*109C>G	NP_006177.1:n.*109C>G
XM_005246621.2:c.*109C>G	XP_005246678.1:n.*109C>G
XM_005246622.2:c.*109C>G	XP_005246679.1:n.*109C>G
XM_005246623.1:c.*109C>G	XP_005246680.1:n.*109C>G
XM_006712553.2:c.*109C>G	XP_006712616.1:n.*109C>G
XM_011511246.1:c.*140C>G	XP_011509548.1:n.*140C>G
NM_173173.2:c.*109C>G	NP_775265.1:n.*109C>G
XM_005246621.4:c.*109C>G	XP_005246678.1:n.*109C>G
XM_006712553.4:c.*109C>G	XP_006712616.1:n.*109C>G
XM_011511246.2:c.*140C>G	XP_011509548.1:n.*140C>G
XM_017004219.2:c.*109C>G	XP_016859708.1:n.*109C>G
XM_017004220.2:c.*109C>G	XP_016859709.1:n.*109C>G
XR_001738751.2:n.2153C>G
XR_001738752.2:n.1975C>G
XR_427087.4:n.2032C>G
NM_006186.4:c.*109C>G MANE Select	NP_006177.1:n.*109C>G
NM_173173.3:c.*109C>G	NP_775265.1:n.*109C>G