Canonical Allele Identifier: CA759313181

Gene: NR4A2

Linked Data

• dbSNP Id: rs1339867307
• gnomAD v4: 2-156325609-G-A
• MyVariant Identifiers: chr2:g.157182121G>A (hg19) ; chr2:g.156325609G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325609G>A , CM000664.2:g.156325609G>A	GRCh38
NC_000002.11:g.157182121G>A , CM000664.1:g.157182121G>A	GRCh37
NC_000002.10:g.156890367G>A	NCBI36
NG_011821.1:g.12167C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*135C>T	ENSP00000514865.1:n.*135C>T
ENST00000700229.1:c.896C>T
ENST00000700230.1:c.1472C>T	ENSP00000514867.1:n.1472C>T
ENST00000700231.1:c.*135C>T	ENSP00000514868.1:n.*135C>T
ENST00000339562.9:c.*135C>T MANE Select	ENSP00000344479.4:n.*135C>T
ENST00000675870.1:c.*443C>T	ENSP00000502739.1:n.*443C>T
ENST00000339562.8:c.*135C>T	ENSP00000344479.4:n.*135C>T
ENST00000409572.5:c.*135C>T	ENSP00000386747.1:n.*135C>T
ENST00000417764.5:c.*443C>T	ENSP00000415632.1:n.*443C>T
ENST00000417972.5:c.*443C>T	ENSP00000394671.1:n.*443C>T
ENST00000426264.5:c.*135C>T	ENSP00000389986.1:n.*135C>T
NM_006186.3:c.*135C>T	NP_006177.1:n.*135C>T
XM_005246621.2:c.*135C>T	XP_005246678.1:n.*135C>T
XM_005246622.2:c.*135C>T	XP_005246679.1:n.*135C>T
XM_005246623.1:c.*135C>T	XP_005246680.1:n.*135C>T
XM_006712553.2:c.*135C>T	XP_006712616.1:n.*135C>T
XM_011511246.1:c.*166C>T	XP_011509548.1:n.*166C>T
NM_173173.2:c.*135C>T	NP_775265.1:n.*135C>T
XM_005246621.4:c.*135C>T	XP_005246678.1:n.*135C>T
XM_006712553.4:c.*135C>T	XP_006712616.1:n.*135C>T
XM_011511246.2:c.*166C>T	XP_011509548.1:n.*166C>T
XM_017004219.2:c.*135C>T	XP_016859708.1:n.*135C>T
XM_017004220.2:c.*135C>T	XP_016859709.1:n.*135C>T
XR_001738751.2:n.2179C>T
XR_001738752.2:n.2001C>T
XR_427087.4:n.2058C>T
NM_006186.4:c.*135C>T MANE Select	NP_006177.1:n.*135C>T
NM_173173.3:c.*135C>T	NP_775265.1:n.*135C>T