Canonical Allele Identifier: CA348681854

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329479-C-A
• MyVariant Identifiers: chr2:g.157185991C>A (hg19) ; chr2:g.156329479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329479C>A , CM000664.2:g.156329479C>A	GRCh38
NC_000002.11:g.157185991C>A , CM000664.1:g.157185991C>A	GRCh37
NC_000002.10:g.156894237C>A	NCBI36
NG_011821.1:g.8297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.579G>T	ENSP00000514865.1:p.Gln193His
ENST00000700230.1:c.141G>T	ENSP00000514867.1:p.Gln47His
ENST00000700231.1:c.708G>T	ENSP00000514868.1:p.Gln236His
ENST00000339562.9:c.708G>T MANE Select	ENSP00000344479.4:p.Gln236His
ENST00000675870.1:c.519G>T	ENSP00000502739.1:p.Gln173His
ENST00000339562.8:c.708G>T	ENSP00000344479.4:p.Gln236His
ENST00000406048.2:c.208+435G>T
ENST00000409108.6:c.708G>T	ENSP00000386993.2:p.Gln236His
ENST00000409572.5:c.708G>T	ENSP00000386747.1:p.Gln236His
ENST00000417764.5:c.519G>T	ENSP00000415632.1:p.Gln173His
ENST00000417972.5:c.519G>T	ENSP00000394671.1:p.Gln173His
ENST00000424077.1:c.708G>T	ENSP00000406808.1:p.Gln236His
ENST00000426264.5:c.519G>T	ENSP00000389986.1:p.Gln173His
ENST00000429376.5:c.519G>T	ENSP00000410952.1:p.Gln173His
NM_006186.3:c.708G>T	NP_006177.1:p.Gln236His
XM_005246621.2:c.741G>T	XP_005246678.1:p.Gln247His
XM_005246622.2:c.519G>T	XP_005246679.1:p.Gln173His
XM_005246623.1:c.519G>T	XP_005246680.1:p.Gln173His
XM_006712553.2:c.741G>T	XP_006712616.1:p.Gln247His
XM_011511246.1:c.741G>T	XP_011509548.1:p.Gln247His
XR_427087.2:n.2914G>T
NM_173173.2:c.519G>T	NP_775265.1:p.Gln173His
XM_005246621.4:c.741G>T	XP_005246678.1:p.Gln247His
XM_006712553.4:c.741G>T	XP_006712616.1:p.Gln247His
XM_011511246.2:c.741G>T	XP_011509548.1:p.Gln247His
XM_017004219.2:c.708G>T	XP_016859708.1:p.Gln236His
XM_017004220.2:c.708G>T	XP_016859709.1:p.Gln236His
XR_001738751.2:n.1076G>T
XR_001738752.2:n.898G>T
XR_427087.4:n.955G>T
NM_006186.4:c.708G>T MANE Select	NP_006177.1:p.Gln236His
NM_173173.3:c.519G>T	NP_775265.1:p.Gln173His