Canonical Allele Identifier: CA1916162

Gene: NR4A2

Linked Data

• dbSNP Id: rs750184164
• ExAC: 2:157182346 C / A
• gnomAD v2: 2-157182346-C-A
• gnomAD v4: 2-156325834-C-A
• MyVariant Identifiers: chr2:g.157182346C>A (hg19) ; chr2:g.156325834C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325834C>A , CM000664.2:g.156325834C>A	GRCh38
NC_000002.11:g.157182346C>A , CM000664.1:g.157182346C>A	GRCh37
NC_000002.10:g.156890592C>A	NCBI36
NG_011821.1:g.11942G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1503G>T	ENSP00000514865.1:p.Gly501=
ENST00000700229.1:c.671G>T
ENST00000700230.1:c.1247G>T	ENSP00000514867.1:n.1247G>T
ENST00000700231.1:c.1632G>T	ENSP00000514868.1:p.Gly544=
ENST00000339562.9:c.1707G>T MANE Select	ENSP00000344479.4:p.Gly569=
ENST00000675870.1:c.*218G>T	ENSP00000502739.1:n.*218G>T
ENST00000339562.8:c.1707G>T	ENSP00000344479.4:p.Gly569=
ENST00000409108.6:c.1603G>T	ENSP00000386993.2:p.Ala535Ser
ENST00000409572.5:c.1707G>T	ENSP00000386747.1:p.Gly569=
ENST00000417764.5:c.*218G>T	ENSP00000415632.1:n.*218G>T
ENST00000417972.5:c.*218G>T	ENSP00000394671.1:n.*218G>T
ENST00000426264.5:c.1518G>T	ENSP00000389986.1:p.Gly506=
ENST00000429376.5:c.1414G>T	ENSP00000410952.1:p.Ala472Ser
NM_006186.3:c.1707G>T	NP_006177.1:p.Gly569=
XM_005246621.2:c.1740G>T	XP_005246678.1:p.Gly580=
XM_005246622.2:c.1518G>T	XP_005246679.1:p.Gly506=
XM_005246623.1:c.1518G>T	XP_005246680.1:p.Gly506=
XM_006712553.2:c.1665G>T	XP_006712616.1:p.Gly555=
XM_011511246.1:c.1636G>T	XP_011509548.1:p.Ala546Ser
NM_173173.2:c.1518G>T	NP_775265.1:p.Gly506=
XM_005246621.4:c.1740G>T	XP_005246678.1:p.Gly580=
XM_006712553.4:c.1665G>T	XP_006712616.1:p.Gly555=
XM_011511246.2:c.1636G>T	XP_011509548.1:p.Ala546Ser
XM_017004219.2:c.1707G>T	XP_016859708.1:p.Gly569=
XM_017004220.2:c.1632G>T	XP_016859709.1:p.Gly544=
XR_001738751.2:n.1954G>T
XR_001738752.2:n.1776G>T
XR_427087.4:n.1833G>T
NM_006186.4:c.1707G>T MANE Select	NP_006177.1:p.Gly569=
NM_173173.3:c.1518G>T	NP_775265.1:p.Gly506=