Canonical Allele Identifier: CA1916385

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 2377115
• ClinVar RCV Id: RCV002673889
• dbSNP Id: rs148826679
• ExAC: 2:157185944 G / T
• gnomAD v2: 2-157185944-G-T
• gnomAD v3: 2-156329432-G-T
• gnomAD v4: 2-156329432-G-T
• MyVariant Identifiers: chr2:g.157185944G>T (hg19) ; chr2:g.156329432G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329432G>T , CM000664.2:g.156329432G>T	GRCh38
NC_000002.11:g.157185944G>T , CM000664.1:g.157185944G>T	GRCh37
NC_000002.10:g.156894190G>T	NCBI36
NG_011821.1:g.8344C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.626C>A	ENSP00000514865.1:p.Pro209Gln
ENST00000700230.1:c.188C>A	ENSP00000514867.1:p.Pro63Gln
ENST00000700231.1:c.755C>A	ENSP00000514868.1:p.Pro252Gln
ENST00000339562.9:c.755C>A MANE Select	ENSP00000344479.4:p.Pro252Gln
ENST00000675870.1:c.566C>A	ENSP00000502739.1:p.Pro189Gln
ENST00000339562.8:c.755C>A	ENSP00000344479.4:p.Pro252Gln
ENST00000406048.2:c.208+482C>A
ENST00000409108.6:c.755C>A	ENSP00000386993.2:p.Pro252Gln
ENST00000409572.5:c.755C>A	ENSP00000386747.1:p.Pro252Gln
ENST00000417764.5:c.566C>A	ENSP00000415632.1:p.Pro189Gln
ENST00000417972.5:c.566C>A	ENSP00000394671.1:p.Pro189Gln
ENST00000424077.1:c.755C>A	ENSP00000406808.1:p.Pro252Gln
ENST00000426264.5:c.566C>A	ENSP00000389986.1:p.Pro189Gln
ENST00000429376.5:c.566C>A	ENSP00000410952.1:p.Pro189Gln
NM_006186.3:c.755C>A	NP_006177.1:p.Pro252Gln
XM_005246621.2:c.788C>A	XP_005246678.1:p.Pro263Gln
XM_005246622.2:c.566C>A	XP_005246679.1:p.Pro189Gln
XM_005246623.1:c.566C>A	XP_005246680.1:p.Pro189Gln
XM_006712553.2:c.788C>A	XP_006712616.1:p.Pro263Gln
XM_011511246.1:c.788C>A	XP_011509548.1:p.Pro263Gln
XR_427087.2:n.2961C>A
NM_173173.2:c.566C>A	NP_775265.1:p.Pro189Gln
XM_005246621.4:c.788C>A	XP_005246678.1:p.Pro263Gln
XM_006712553.4:c.788C>A	XP_006712616.1:p.Pro263Gln
XM_011511246.2:c.788C>A	XP_011509548.1:p.Pro263Gln
XM_017004219.2:c.755C>A	XP_016859708.1:p.Pro252Gln
XM_017004220.2:c.755C>A	XP_016859709.1:p.Pro252Gln
XR_001738751.2:n.1123C>A
XR_001738752.2:n.945C>A
XR_427087.4:n.1002C>A
NM_006186.4:c.755C>A MANE Select	NP_006177.1:p.Pro252Gln
NM_173173.3:c.566C>A	NP_775265.1:p.Pro189Gln