Canonical Allele Identifier: CA1916178

Gene: NR4A2

Linked Data

• dbSNP Id: rs201003462
• ExAC: 2:157182438 C / T
• gnomAD v2: 2-157182438-C-T
• gnomAD v3: 2-156325926-C-T
• gnomAD v4: 2-156325926-C-T
• MyVariant Identifiers: chr2:g.157182438C>T (hg19) ; chr2:g.156325926C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325926C>T , CM000664.2:g.156325926C>T	GRCh38
NC_000002.11:g.157182438C>T , CM000664.1:g.157182438C>T	GRCh37
NC_000002.10:g.156890684C>T	NCBI36
NG_011821.1:g.11850G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1411G>A	ENSP00000514865.1:p.Val471Met
ENST00000700229.1:c.579G>A
ENST00000700230.1:c.1155G>A	ENSP00000514867.1:n.1155G>A
ENST00000700231.1:c.1540G>A	ENSP00000514868.1:p.Val514Met
ENST00000339562.9:c.1615G>A MANE Select	ENSP00000344479.4:p.Val539Met
ENST00000675870.1:c.*126G>A	ENSP00000502739.1:n.*126G>A
ENST00000339562.8:c.1615G>A	ENSP00000344479.4:p.Val539Met
ENST00000409108.6:c.1511G>A	ENSP00000386993.2:p.Arg504His
ENST00000409572.5:c.1615G>A	ENSP00000386747.1:p.Val539Met
ENST00000417764.5:c.*126G>A	ENSP00000415632.1:n.*126G>A
ENST00000417972.5:c.*126G>A	ENSP00000394671.1:n.*126G>A
ENST00000426264.5:c.1426G>A	ENSP00000389986.1:p.Val476Met
ENST00000429376.5:c.1322G>A	ENSP00000410952.1:p.Arg441His
NM_006186.3:c.1615G>A	NP_006177.1:p.Val539Met
XM_005246621.2:c.1648G>A	XP_005246678.1:p.Val550Met
XM_005246622.2:c.1426G>A	XP_005246679.1:p.Val476Met
XM_005246623.1:c.1426G>A	XP_005246680.1:p.Val476Met
XM_006712553.2:c.1573G>A	XP_006712616.1:p.Val525Met
XM_011511246.1:c.1544G>A	XP_011509548.1:p.Arg515His
NM_173173.2:c.1426G>A	NP_775265.1:p.Val476Met
XM_005246621.4:c.1648G>A	XP_005246678.1:p.Val550Met
XM_006712553.4:c.1573G>A	XP_006712616.1:p.Val525Met
XM_011511246.2:c.1544G>A	XP_011509548.1:p.Arg515His
XM_017004219.2:c.1615G>A	XP_016859708.1:p.Val539Met
XM_017004220.2:c.1540G>A	XP_016859709.1:p.Val514Met
XR_001738751.2:n.1862G>A
XR_001738752.2:n.1684G>A
XR_427087.4:n.1741G>A
NM_006186.4:c.1615G>A MANE Select	NP_006177.1:p.Val539Met
NM_173173.3:c.1426G>A	NP_775265.1:p.Val476Met