Canonical Allele Identifier: CA348679726

Gene: NR4A2

Linked Data

• dbSNP Id: rs1686623233
• gnomAD v4: 2-156325934-T-C
• MyVariant Identifiers: chr2:g.157182446T>C (hg19) ; chr2:g.156325934T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325934T>C , CM000664.2:g.156325934T>C	GRCh38
NC_000002.11:g.157182446T>C , CM000664.1:g.157182446T>C	GRCh37
NC_000002.10:g.156890692T>C	NCBI36
NG_011821.1:g.11842A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1403A>G	ENSP00000514865.1:p.Lys468Arg
ENST00000700229.1:c.571A>G
ENST00000700230.1:c.1147A>G	ENSP00000514867.1:n.1147A>G
ENST00000700231.1:c.1532A>G	ENSP00000514868.1:p.Lys511Arg
ENST00000339562.9:c.1607A>G MANE Select	ENSP00000344479.4:p.Lys536Arg
ENST00000675870.1:c.*118A>G	ENSP00000502739.1:n.*118A>G
ENST00000339562.8:c.1607A>G	ENSP00000344479.4:p.Lys536Arg
ENST00000409108.6:c.1503A>G	ENSP00000386993.2:p.Gln501=
ENST00000409572.5:c.1607A>G	ENSP00000386747.1:p.Lys536Arg
ENST00000417764.5:c.*118A>G	ENSP00000415632.1:n.*118A>G
ENST00000417972.5:c.*118A>G	ENSP00000394671.1:n.*118A>G
ENST00000426264.5:c.1418A>G	ENSP00000389986.1:p.Lys473Arg
ENST00000429376.5:c.1314A>G	ENSP00000410952.1:p.Gln438=
NM_006186.3:c.1607A>G	NP_006177.1:p.Lys536Arg
XM_005246621.2:c.1640A>G	XP_005246678.1:p.Lys547Arg
XM_005246622.2:c.1418A>G	XP_005246679.1:p.Lys473Arg
XM_005246623.1:c.1418A>G	XP_005246680.1:p.Lys473Arg
XM_006712553.2:c.1565A>G	XP_006712616.1:p.Lys522Arg
XM_011511246.1:c.1536A>G	XP_011509548.1:p.Gln512=
NM_173173.2:c.1418A>G	NP_775265.1:p.Lys473Arg
XM_005246621.4:c.1640A>G	XP_005246678.1:p.Lys547Arg
XM_006712553.4:c.1565A>G	XP_006712616.1:p.Lys522Arg
XM_011511246.2:c.1536A>G	XP_011509548.1:p.Gln512=
XM_017004219.2:c.1607A>G	XP_016859708.1:p.Lys536Arg
XM_017004220.2:c.1532A>G	XP_016859709.1:p.Lys511Arg
XR_001738751.2:n.1854A>G
XR_001738752.2:n.1676A>G
XR_427087.4:n.1733A>G
NM_006186.4:c.1607A>G MANE Select	NP_006177.1:p.Lys536Arg
NM_173173.3:c.1418A>G	NP_775265.1:p.Lys473Arg