Canonical Allele Identifier: CA348679625

Gene: NR4A2

Linked Data

• dbSNP Id: rs1457299588
• gnomAD v2: 2-157182407-G-T
• gnomAD v4: 2-156325895-G-T
• MyVariant Identifiers: chr2:g.157182407G>T (hg19) ; chr2:g.156325895G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325895G>T , CM000664.2:g.156325895G>T	GRCh38
NC_000002.11:g.157182407G>T , CM000664.1:g.157182407G>T	GRCh37
NC_000002.10:g.156890653G>T	NCBI36
NG_011821.1:g.11881C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1442C>A	ENSP00000514865.1:p.Pro481His
ENST00000700229.1:c.610C>A
ENST00000700230.1:c.1186C>A	ENSP00000514867.1:n.1186C>A
ENST00000700231.1:c.1571C>A	ENSP00000514868.1:p.Pro524His
ENST00000339562.9:c.1646C>A MANE Select	ENSP00000344479.4:p.Pro549His
ENST00000675870.1:c.*157C>A	ENSP00000502739.1:n.*157C>A
ENST00000339562.8:c.1646C>A	ENSP00000344479.4:p.Pro549His
ENST00000409108.6:c.1542C>A	ENSP00000386993.2:p.Pro514=
ENST00000409572.5:c.1646C>A	ENSP00000386747.1:p.Pro549His
ENST00000417764.5:c.*157C>A	ENSP00000415632.1:n.*157C>A
ENST00000417972.5:c.*157C>A	ENSP00000394671.1:n.*157C>A
ENST00000426264.5:c.1457C>A	ENSP00000389986.1:p.Pro486His
ENST00000429376.5:c.1353C>A	ENSP00000410952.1:p.Pro451=
NM_006186.3:c.1646C>A	NP_006177.1:p.Pro549His
XM_005246621.2:c.1679C>A	XP_005246678.1:p.Pro560His
XM_005246622.2:c.1457C>A	XP_005246679.1:p.Pro486His
XM_005246623.1:c.1457C>A	XP_005246680.1:p.Pro486His
XM_006712553.2:c.1604C>A	XP_006712616.1:p.Pro535His
XM_011511246.1:c.1575C>A	XP_011509548.1:p.Pro525=
NM_173173.2:c.1457C>A	NP_775265.1:p.Pro486His
XM_005246621.4:c.1679C>A	XP_005246678.1:p.Pro560His
XM_006712553.4:c.1604C>A	XP_006712616.1:p.Pro535His
XM_011511246.2:c.1575C>A	XP_011509548.1:p.Pro525=
XM_017004219.2:c.1646C>A	XP_016859708.1:p.Pro549His
XM_017004220.2:c.1571C>A	XP_016859709.1:p.Pro524His
XR_001738751.2:n.1893C>A
XR_001738752.2:n.1715C>A
XR_427087.4:n.1772C>A
NM_006186.4:c.1646C>A MANE Select	NP_006177.1:p.Pro549His
NM_173173.3:c.1457C>A	NP_775265.1:p.Pro486His