Canonical Allele Identifier: CA348680052

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686635630
• gnomAD v3: 2-156326197-A-C
• gnomAD v4: 2-156326197-A-C
• MyVariant Identifiers: chr2:g.157182709A>C (hg19) ; chr2:g.156326197A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326197A>C , CM000664.2:g.156326197A>C	GRCh38
NC_000002.11:g.157182709A>C , CM000664.1:g.157182709A>C	GRCh37
NC_000002.10:g.156890955A>C	NCBI36
NG_011821.1:g.11579T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1289T>G	ENSP00000514865.1:p.Ile430Ser
ENST00000700229.1:c.457T>G
ENST00000700230.1:c.1033T>G	ENSP00000514867.1:n.1033T>G
ENST00000700231.1:c.1418T>G	ENSP00000514868.1:p.Ile473Ser
ENST00000339562.9:c.1493T>G MANE Select	ENSP00000344479.4:p.Ile498Ser
ENST00000675870.1:c.*4T>G	ENSP00000502739.1:n.*4T>G
ENST00000339562.8:c.1493T>G	ENSP00000344479.4:p.Ile498Ser
ENST00000409108.6:c.1389T>G	ENSP00000386993.2:p.His463Gln
ENST00000409572.5:c.1493T>G	ENSP00000386747.1:p.Ile498Ser
ENST00000417764.5:c.*4T>G	ENSP00000415632.1:n.*4T>G
ENST00000417972.5:c.*4T>G	ENSP00000394671.1:n.*4T>G
ENST00000426264.5:c.1304T>G	ENSP00000389986.1:p.Ile435Ser
ENST00000429376.5:c.1200T>G	ENSP00000410952.1:p.His400Gln
NM_006186.3:c.1493T>G	NP_006177.1:p.Ile498Ser
XM_005246621.2:c.1526T>G	XP_005246678.1:p.Ile509Ser
XM_005246622.2:c.1304T>G	XP_005246679.1:p.Ile435Ser
XM_005246623.1:c.1304T>G	XP_005246680.1:p.Ile435Ser
XM_006712553.2:c.1451T>G	XP_006712616.1:p.Ile484Ser
XM_011511246.1:c.1422T>G	XP_011509548.1:p.His474Gln
XR_427087.2:n.3578T>G
NM_173173.2:c.1304T>G	NP_775265.1:p.Ile435Ser
XM_005246621.4:c.1526T>G	XP_005246678.1:p.Ile509Ser
XM_006712553.4:c.1451T>G	XP_006712616.1:p.Ile484Ser
XM_011511246.2:c.1422T>G	XP_011509548.1:p.His474Gln
XM_017004219.2:c.1493T>G	XP_016859708.1:p.Ile498Ser
XM_017004220.2:c.1418T>G	XP_016859709.1:p.Ile473Ser
XR_001738751.2:n.1740T>G
XR_001738752.2:n.1562T>G
XR_427087.4:n.1619T>G
NM_006186.4:c.1493T>G MANE Select	NP_006177.1:p.Ile498Ser
NM_173173.3:c.1304T>G	NP_775265.1:p.Ile435Ser