Canonical Allele Identifier: CA1916392

Gene: NR4A2

Linked Data

• dbSNP Id: rs751045429
• ExAC: 2:157185976 A / G
• gnomAD v4: 2-156329464-A-G
• MyVariant Identifiers: chr2:g.157185976A>G (hg19) ; chr2:g.156329464A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329464A>G , CM000664.2:g.156329464A>G	GRCh38
NC_000002.11:g.157185976A>G , CM000664.1:g.157185976A>G	GRCh37
NC_000002.10:g.156894222A>G	NCBI36
NG_011821.1:g.8312T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.594T>C	ENSP00000514865.1:p.Ser198=
ENST00000700230.1:c.156T>C	ENSP00000514867.1:p.Ser52=
ENST00000700231.1:c.723T>C	ENSP00000514868.1:p.Ser241=
ENST00000339562.9:c.723T>C MANE Select	ENSP00000344479.4:p.Ser241=
ENST00000675870.1:c.534T>C	ENSP00000502739.1:p.Ser178=
ENST00000339562.8:c.723T>C	ENSP00000344479.4:p.Ser241=
ENST00000406048.2:c.208+450T>C
ENST00000409108.6:c.723T>C	ENSP00000386993.2:p.Ser241=
ENST00000409572.5:c.723T>C	ENSP00000386747.1:p.Ser241=
ENST00000417764.5:c.534T>C	ENSP00000415632.1:p.Ser178=
ENST00000417972.5:c.534T>C	ENSP00000394671.1:p.Ser178=
ENST00000424077.1:c.723T>C	ENSP00000406808.1:p.Ser241=
ENST00000426264.5:c.534T>C	ENSP00000389986.1:p.Ser178=
ENST00000429376.5:c.534T>C	ENSP00000410952.1:p.Ser178=
NM_006186.3:c.723T>C	NP_006177.1:p.Ser241=
XM_005246621.2:c.756T>C	XP_005246678.1:p.Ser252=
XM_005246622.2:c.534T>C	XP_005246679.1:p.Ser178=
XM_005246623.1:c.534T>C	XP_005246680.1:p.Ser178=
XM_006712553.2:c.756T>C	XP_006712616.1:p.Ser252=
XM_011511246.1:c.756T>C	XP_011509548.1:p.Ser252=
XR_427087.2:n.2929T>C
NM_173173.2:c.534T>C	NP_775265.1:p.Ser178=
XM_005246621.4:c.756T>C	XP_005246678.1:p.Ser252=
XM_006712553.4:c.756T>C	XP_006712616.1:p.Ser252=
XM_011511246.2:c.756T>C	XP_011509548.1:p.Ser252=
XM_017004219.2:c.723T>C	XP_016859708.1:p.Ser241=
XM_017004220.2:c.723T>C	XP_016859709.1:p.Ser241=
XR_001738751.2:n.1091T>C
XR_001738752.2:n.913T>C
XR_427087.4:n.970T>C
NM_006186.4:c.723T>C MANE Select	NP_006177.1:p.Ser241=
NM_173173.3:c.534T>C	NP_775265.1:p.Ser178=