Canonical Allele Identifier: CA1916205

Gene: NR4A2

Linked Data

• dbSNP Id: rs754453436
• ExAC: 2:157182686 T / C
• gnomAD v2: 2-157182686-T-C
• gnomAD v3: 2-156326174-T-C
• gnomAD v4: 2-156326174-T-C
• MyVariant Identifiers: chr2:g.157182686T>C (hg19) ; chr2:g.156326174T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326174T>C , CM000664.2:g.156326174T>C	GRCh38
NC_000002.11:g.157182686T>C , CM000664.1:g.157182686T>C	GRCh37
NC_000002.10:g.156890932T>C	NCBI36
NG_011821.1:g.11602A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1312A>G	ENSP00000514865.1:p.Ile438Val
ENST00000700229.1:c.480A>G
ENST00000700230.1:c.1056A>G	ENSP00000514867.1:n.1056A>G
ENST00000700231.1:c.1441A>G	ENSP00000514868.1:p.Ile481Val
ENST00000339562.9:c.1516A>G MANE Select	ENSP00000344479.4:p.Ile506Val
ENST00000675870.1:c.*27A>G	ENSP00000502739.1:n.*27A>G
ENST00000339562.8:c.1516A>G	ENSP00000344479.4:p.Ile506Val
ENST00000409108.6:c.1412A>G	ENSP00000386993.2:p.His471Arg
ENST00000409572.5:c.1516A>G	ENSP00000386747.1:p.Ile506Val
ENST00000417764.5:c.*27A>G	ENSP00000415632.1:n.*27A>G
ENST00000417972.5:c.*27A>G	ENSP00000394671.1:n.*27A>G
ENST00000426264.5:c.1327A>G	ENSP00000389986.1:p.Ile443Val
ENST00000429376.5:c.1223A>G	ENSP00000410952.1:p.His408Arg
NM_006186.3:c.1516A>G	NP_006177.1:p.Ile506Val
XM_005246621.2:c.1549A>G	XP_005246678.1:p.Ile517Val
XM_005246622.2:c.1327A>G	XP_005246679.1:p.Ile443Val
XM_005246623.1:c.1327A>G	XP_005246680.1:p.Ile443Val
XM_006712553.2:c.1474A>G	XP_006712616.1:p.Ile492Val
XM_011511246.1:c.1445A>G	XP_011509548.1:p.His482Arg
XR_427087.2:n.3601A>G
NM_173173.2:c.1327A>G	NP_775265.1:p.Ile443Val
XM_005246621.4:c.1549A>G	XP_005246678.1:p.Ile517Val
XM_006712553.4:c.1474A>G	XP_006712616.1:p.Ile492Val
XM_011511246.2:c.1445A>G	XP_011509548.1:p.His482Arg
XM_017004219.2:c.1516A>G	XP_016859708.1:p.Ile506Val
XM_017004220.2:c.1441A>G	XP_016859709.1:p.Ile481Val
XR_001738751.2:n.1763A>G
XR_001738752.2:n.1585A>G
XR_427087.4:n.1642A>G
NM_006186.4:c.1516A>G MANE Select	NP_006177.1:p.Ile506Val
NM_173173.3:c.1327A>G	NP_775265.1:p.Ile443Val