Canonical Allele Identifier: CA1916202

Gene: NR4A2

Linked Data

• dbSNP Id: rs752278607
• ExAC: 2:157182671 T / C
• gnomAD v2: 2-157182671-T-C
• gnomAD v3: 2-156326159-T-C
• gnomAD v4: 2-156326159-T-C
• MyVariant Identifiers: chr2:g.157182671T>C (hg19) ; chr2:g.156326159T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326159T>C , CM000664.2:g.156326159T>C	GRCh38
NC_000002.11:g.157182671T>C , CM000664.1:g.157182671T>C	GRCh37
NC_000002.10:g.156890917T>C	NCBI36
NG_011821.1:g.11617A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1327A>G	ENSP00000514865.1:p.Met443Val
ENST00000700229.1:c.495A>G
ENST00000700230.1:c.1071A>G	ENSP00000514867.1:n.1071A>G
ENST00000700231.1:c.1456A>G	ENSP00000514868.1:p.Met486Val
ENST00000339562.9:c.1531A>G MANE Select	ENSP00000344479.4:p.Met511Val
ENST00000675870.1:c.*42A>G	ENSP00000502739.1:n.*42A>G
ENST00000339562.8:c.1531A>G	ENSP00000344479.4:p.Met511Val
ENST00000409108.6:c.1427A>G	ENSP00000386993.2:p.Tyr476Cys
ENST00000409572.5:c.1531A>G	ENSP00000386747.1:p.Met511Val
ENST00000417764.5:c.*42A>G	ENSP00000415632.1:n.*42A>G
ENST00000417972.5:c.*42A>G	ENSP00000394671.1:n.*42A>G
ENST00000426264.5:c.1342A>G	ENSP00000389986.1:p.Met448Val
ENST00000429376.5:c.1238A>G	ENSP00000410952.1:p.Tyr413Cys
NM_006186.3:c.1531A>G	NP_006177.1:p.Met511Val
XM_005246621.2:c.1564A>G	XP_005246678.1:p.Met522Val
XM_005246622.2:c.1342A>G	XP_005246679.1:p.Met448Val
XM_005246623.1:c.1342A>G	XP_005246680.1:p.Met448Val
XM_006712553.2:c.1489A>G	XP_006712616.1:p.Met497Val
XM_011511246.1:c.1460A>G	XP_011509548.1:p.Tyr487Cys
XR_427087.2:n.3616A>G
NM_173173.2:c.1342A>G	NP_775265.1:p.Met448Val
XM_005246621.4:c.1564A>G	XP_005246678.1:p.Met522Val
XM_006712553.4:c.1489A>G	XP_006712616.1:p.Met497Val
XM_011511246.2:c.1460A>G	XP_011509548.1:p.Tyr487Cys
XM_017004219.2:c.1531A>G	XP_016859708.1:p.Met511Val
XM_017004220.2:c.1456A>G	XP_016859709.1:p.Met486Val
XR_001738751.2:n.1778A>G
XR_001738752.2:n.1600A>G
XR_427087.4:n.1657A>G
NM_006186.4:c.1531A>G MANE Select	NP_006177.1:p.Met511Val
NM_173173.3:c.1342A>G	NP_775265.1:p.Met448Val