Canonical Allele Identifier: CA348680001

Gene: NR4A2

Linked Data

• dbSNP Id: rs1204331889
• gnomAD v2: 2-157182689-A-C
• gnomAD v3: 2-156326177-A-C
• gnomAD v4: 2-156326177-A-C
• MyVariant Identifiers: chr2:g.157182689A>C (hg19) ; chr2:g.156326177A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326177A>C , CM000664.2:g.156326177A>C	GRCh38
NC_000002.11:g.157182689A>C , CM000664.1:g.157182689A>C	GRCh37
NC_000002.10:g.156890935A>C	NCBI36
NG_011821.1:g.11599T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1309T>G	ENSP00000514865.1:p.Cys437Gly
ENST00000700229.1:c.477T>G
ENST00000700230.1:c.1053T>G	ENSP00000514867.1:n.1053T>G
ENST00000700231.1:c.1438T>G	ENSP00000514868.1:p.Cys480Gly
ENST00000339562.9:c.1513T>G MANE Select	ENSP00000344479.4:p.Cys505Gly
ENST00000675870.1:c.*24T>G	ENSP00000502739.1:n.*24T>G
ENST00000339562.8:c.1513T>G	ENSP00000344479.4:p.Cys505Gly
ENST00000409108.6:c.1409T>G	ENSP00000386993.2:p.Leu470Arg
ENST00000409572.5:c.1513T>G	ENSP00000386747.1:p.Cys505Gly
ENST00000417764.5:c.*24T>G	ENSP00000415632.1:n.*24T>G
ENST00000417972.5:c.*24T>G	ENSP00000394671.1:n.*24T>G
ENST00000426264.5:c.1324T>G	ENSP00000389986.1:p.Cys442Gly
ENST00000429376.5:c.1220T>G	ENSP00000410952.1:p.Leu407Arg
NM_006186.3:c.1513T>G	NP_006177.1:p.Cys505Gly
XM_005246621.2:c.1546T>G	XP_005246678.1:p.Cys516Gly
XM_005246622.2:c.1324T>G	XP_005246679.1:p.Cys442Gly
XM_005246623.1:c.1324T>G	XP_005246680.1:p.Cys442Gly
XM_006712553.2:c.1471T>G	XP_006712616.1:p.Cys491Gly
XM_011511246.1:c.1442T>G	XP_011509548.1:p.Leu481Arg
XR_427087.2:n.3598T>G
NM_173173.2:c.1324T>G	NP_775265.1:p.Cys442Gly
XM_005246621.4:c.1546T>G	XP_005246678.1:p.Cys516Gly
XM_006712553.4:c.1471T>G	XP_006712616.1:p.Cys491Gly
XM_011511246.2:c.1442T>G	XP_011509548.1:p.Leu481Arg
XM_017004219.2:c.1513T>G	XP_016859708.1:p.Cys505Gly
XM_017004220.2:c.1438T>G	XP_016859709.1:p.Cys480Gly
XR_001738751.2:n.1760T>G
XR_001738752.2:n.1582T>G
XR_427087.4:n.1639T>G
NM_006186.4:c.1513T>G MANE Select	NP_006177.1:p.Cys505Gly
NM_173173.3:c.1324T>G	NP_775265.1:p.Cys442Gly