Canonical Allele Identifier: CA277455

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 212706
• ClinVar RCV Id: RCV000195213
• dbSNP Id: rs797046133
• gnomAD v4: 2-156329830-C-A
• MyVariant Identifiers: chr2:g.157186342C>A (hg19) ; chr2:g.156329830C>A (hg38)
• PubMed: PMID:26352270

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329830C>A , CM000664.2:g.156329830C>A	GRCh38
NC_000002.11:g.157186342C>A , CM000664.1:g.157186342C>A	GRCh37
NC_000002.10:g.156894588C>A	NCBI36
NG_011821.1:g.7946G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000421709.2:c.168G>T	ENSP00000388120.2:p.Ser56=
ENST00000700228.1:c.228G>T	ENSP00000514865.1:p.Ser76=
ENST00000700231.1:c.357G>T	ENSP00000514868.1:p.Ser119=
ENST00000339562.9:c.357G>T MANE Select	ENSP00000344479.4:p.Ser119=
ENST00000675870.1:c.168G>T	ENSP00000502739.1:p.Ser56=
ENST00000339562.8:c.357G>T	ENSP00000344479.4:p.Ser119=
ENST00000406048.2:c.208+84G>T
ENST00000409108.6:c.357G>T	ENSP00000386993.2:p.Ser119=
ENST00000409572.5:c.357G>T	ENSP00000386747.1:p.Ser119=
ENST00000417764.5:c.168G>T	ENSP00000415632.1:p.Ser56=
ENST00000417972.5:c.168G>T	ENSP00000394671.1:p.Ser56=
ENST00000421709.1:c.168G>T	ENSP00000388120.1:p.Ser56=
ENST00000424077.1:c.357G>T	ENSP00000406808.1:p.Ser119=
ENST00000426264.5:c.168G>T	ENSP00000389986.1:p.Ser56=
ENST00000429376.5:c.168G>T	ENSP00000410952.1:p.Ser56=
NM_006186.3:c.357G>T	NP_006177.1:p.Ser119=
XM_005246621.2:c.390G>T	XP_005246678.1:p.Ser130=
XM_005246622.2:c.168G>T	XP_005246679.1:p.Ser56=
XM_005246623.1:c.168G>T	XP_005246680.1:p.Ser56=
XM_006712553.2:c.390G>T	XP_006712616.1:p.Ser130=
XM_011511246.1:c.390G>T	XP_011509548.1:p.Ser130=
XR_427087.2:n.2563G>T
NM_173173.2:c.168G>T	NP_775265.1:p.Ser56=
XM_005246621.4:c.390G>T	XP_005246678.1:p.Ser130=
XM_006712553.4:c.390G>T	XP_006712616.1:p.Ser130=
XM_011511246.2:c.390G>T	XP_011509548.1:p.Ser130=
XM_017004219.2:c.357G>T	XP_016859708.1:p.Ser119=
XM_017004220.2:c.357G>T	XP_016859709.1:p.Ser119=
XR_001738751.2:n.725G>T
XR_001738752.2:n.547G>T
XR_427087.4:n.604G>T
NM_006186.4:c.357G>T MANE Select	NP_006177.1:p.Ser119=
NM_173173.3:c.168G>T	NP_775265.1:p.Ser56=