Canonical Allele Identifier: CA1916406

Gene: NR4A2

Linked Data

• dbSNP Id: rs370797040
• ExAC: 2:157186043 G / A
• gnomAD v2: 2-157186043-G-A
• gnomAD v3: 2-156329531-G-A
• gnomAD v4: 2-156329531-G-A
• MyVariant Identifiers: chr2:g.157186043G>A (hg19) ; chr2:g.156329531G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329531G>A , CM000664.2:g.156329531G>A	GRCh38
NC_000002.11:g.157186043G>A , CM000664.1:g.157186043G>A	GRCh37
NC_000002.10:g.156894289G>A	NCBI36
NG_011821.1:g.8245C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.467C>T	ENSP00000388120.2:p.Ala156Val
ENST00000700228.1:c.527C>T	ENSP00000514865.1:p.Ala176Val
ENST00000700230.1:c.89C>T	ENSP00000514867.1:p.Ala30Val
ENST00000700231.1:c.656C>T	ENSP00000514868.1:p.Ala219Val
ENST00000339562.9:c.656C>T MANE Select	ENSP00000344479.4:p.Ala219Val
ENST00000675870.1:c.467C>T	ENSP00000502739.1:p.Ala156Val
ENST00000339562.8:c.656C>T	ENSP00000344479.4:p.Ala219Val
ENST00000406048.2:c.208+383C>T
ENST00000409108.6:c.656C>T	ENSP00000386993.2:p.Ala219Val
ENST00000409572.5:c.656C>T	ENSP00000386747.1:p.Ala219Val
ENST00000417764.5:c.467C>T	ENSP00000415632.1:p.Ala156Val
ENST00000417972.5:c.467C>T	ENSP00000394671.1:p.Ala156Val
ENST00000424077.1:c.656C>T	ENSP00000406808.1:p.Ala219Val
ENST00000426264.5:c.467C>T	ENSP00000389986.1:p.Ala156Val
ENST00000429376.5:c.467C>T	ENSP00000410952.1:p.Ala156Val
NM_006186.3:c.656C>T	NP_006177.1:p.Ala219Val
XM_005246621.2:c.689C>T	XP_005246678.1:p.Ala230Val
XM_005246622.2:c.467C>T	XP_005246679.1:p.Ala156Val
XM_005246623.1:c.467C>T	XP_005246680.1:p.Ala156Val
XM_006712553.2:c.689C>T	XP_006712616.1:p.Ala230Val
XM_011511246.1:c.689C>T	XP_011509548.1:p.Ala230Val
XR_427087.2:n.2862C>T
NM_173173.2:c.467C>T	NP_775265.1:p.Ala156Val
XM_005246621.4:c.689C>T	XP_005246678.1:p.Ala230Val
XM_006712553.4:c.689C>T	XP_006712616.1:p.Ala230Val
XM_011511246.2:c.689C>T	XP_011509548.1:p.Ala230Val
XM_017004219.2:c.656C>T	XP_016859708.1:p.Ala219Val
XM_017004220.2:c.656C>T	XP_016859709.1:p.Ala219Val
XR_001738751.2:n.1024C>T
XR_001738752.2:n.846C>T
XR_427087.4:n.903C>T
NM_006186.4:c.656C>T MANE Select	NP_006177.1:p.Ala219Val
NM_173173.3:c.467C>T	NP_775265.1:p.Ala156Val