Canonical Allele Identifier: CA348680041

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686634093
• gnomAD v3: 2-156326191-A-G
• gnomAD v4: 2-156326191-A-G
• MyVariant Identifiers: chr2:g.157182703A>G (hg19) ; chr2:g.156326191A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326191A>G , CM000664.2:g.156326191A>G	GRCh38
NC_000002.11:g.157182703A>G , CM000664.1:g.157182703A>G	GRCh37
NC_000002.10:g.156890949A>G	NCBI36
NG_011821.1:g.11585T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1295T>C	ENSP00000514865.1:p.Ile432Thr
ENST00000700229.1:c.463T>C
ENST00000700230.1:c.1039T>C	ENSP00000514867.1:n.1039T>C
ENST00000700231.1:c.1424T>C	ENSP00000514868.1:p.Ile475Thr
ENST00000339562.9:c.1499T>C MANE Select	ENSP00000344479.4:p.Ile500Thr
ENST00000675870.1:c.*10T>C	ENSP00000502739.1:n.*10T>C
ENST00000339562.8:c.1499T>C	ENSP00000344479.4:p.Ile500Thr
ENST00000409108.6:c.1395T>C	ENSP00000386993.2:p.His465=
ENST00000409572.5:c.1499T>C	ENSP00000386747.1:p.Ile500Thr
ENST00000417764.5:c.*10T>C	ENSP00000415632.1:n.*10T>C
ENST00000417972.5:c.*10T>C	ENSP00000394671.1:n.*10T>C
ENST00000426264.5:c.1310T>C	ENSP00000389986.1:p.Ile437Thr
ENST00000429376.5:c.1206T>C	ENSP00000410952.1:p.His402=
NM_006186.3:c.1499T>C	NP_006177.1:p.Ile500Thr
XM_005246621.2:c.1532T>C	XP_005246678.1:p.Ile511Thr
XM_005246622.2:c.1310T>C	XP_005246679.1:p.Ile437Thr
XM_005246623.1:c.1310T>C	XP_005246680.1:p.Ile437Thr
XM_006712553.2:c.1457T>C	XP_006712616.1:p.Ile486Thr
XM_011511246.1:c.1428T>C	XP_011509548.1:p.His476=
XR_427087.2:n.3584T>C
NM_173173.2:c.1310T>C	NP_775265.1:p.Ile437Thr
XM_005246621.4:c.1532T>C	XP_005246678.1:p.Ile511Thr
XM_006712553.4:c.1457T>C	XP_006712616.1:p.Ile486Thr
XM_011511246.2:c.1428T>C	XP_011509548.1:p.His476=
XM_017004219.2:c.1499T>C	XP_016859708.1:p.Ile500Thr
XM_017004220.2:c.1424T>C	XP_016859709.1:p.Ile475Thr
XR_001738751.2:n.1746T>C
XR_001738752.2:n.1568T>C
XR_427087.4:n.1625T>C
NM_006186.4:c.1499T>C MANE Select	NP_006177.1:p.Ile500Thr
NM_173173.3:c.1310T>C	NP_775265.1:p.Ile437Thr