Canonical Allele Identifier: CA1916405

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 331662
• ClinVar RCV Id: RCV000357837 ; RCV003430837
• dbSNP Id: rs769677341
• ExAC: 2:157186042 A / G
• gnomAD v2: 2-157186042-A-G
• gnomAD v3: 2-156329530-A-G
• gnomAD v4: 2-156329530-A-G
• MyVariant Identifiers: chr2:g.157186042A>G (hg19) ; chr2:g.156329530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329530A>G , CM000664.2:g.156329530A>G	GRCh38
NC_000002.11:g.157186042A>G , CM000664.1:g.157186042A>G	GRCh37
NC_000002.10:g.156894288A>G	NCBI36
NG_011821.1:g.8246T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.468T>C	ENSP00000388120.2:p.Ala156=
ENST00000700228.1:c.528T>C	ENSP00000514865.1:p.Ala176=
ENST00000700230.1:c.90T>C	ENSP00000514867.1:p.Ala30=
ENST00000700231.1:c.657T>C	ENSP00000514868.1:p.Ala219=
ENST00000339562.9:c.657T>C MANE Select	ENSP00000344479.4:p.Ala219=
ENST00000675870.1:c.468T>C	ENSP00000502739.1:p.Ala156=
ENST00000339562.8:c.657T>C	ENSP00000344479.4:p.Ala219=
ENST00000406048.2:c.208+384T>C
ENST00000409108.6:c.657T>C	ENSP00000386993.2:p.Ala219=
ENST00000409572.5:c.657T>C	ENSP00000386747.1:p.Ala219=
ENST00000417764.5:c.468T>C	ENSP00000415632.1:p.Ala156=
ENST00000417972.5:c.468T>C	ENSP00000394671.1:p.Ala156=
ENST00000424077.1:c.657T>C	ENSP00000406808.1:p.Ala219=
ENST00000426264.5:c.468T>C	ENSP00000389986.1:p.Ala156=
ENST00000429376.5:c.468T>C	ENSP00000410952.1:p.Ala156=
NM_006186.3:c.657T>C	NP_006177.1:p.Ala219=
XM_005246621.2:c.690T>C	XP_005246678.1:p.Ala230=
XM_005246622.2:c.468T>C	XP_005246679.1:p.Ala156=
XM_005246623.1:c.468T>C	XP_005246680.1:p.Ala156=
XM_006712553.2:c.690T>C	XP_006712616.1:p.Ala230=
XM_011511246.1:c.690T>C	XP_011509548.1:p.Ala230=
XR_427087.2:n.2863T>C
NM_173173.2:c.468T>C	NP_775265.1:p.Ala156=
XM_005246621.4:c.690T>C	XP_005246678.1:p.Ala230=
XM_006712553.4:c.690T>C	XP_006712616.1:p.Ala230=
XM_011511246.2:c.690T>C	XP_011509548.1:p.Ala230=
XM_017004219.2:c.657T>C	XP_016859708.1:p.Ala219=
XM_017004220.2:c.657T>C	XP_016859709.1:p.Ala219=
XR_001738751.2:n.1025T>C
XR_001738752.2:n.847T>C
XR_427087.4:n.904T>C
NM_006186.4:c.657T>C MANE Select	NP_006177.1:p.Ala219=
NM_173173.3:c.468T>C	NP_775265.1:p.Ala156=