Canonical Allele Identifier: CA59154807

Gene: NR4A2

Linked Data

• dbSNP Id: rs780261821
• gnomAD v4: 2-156326196-G-C
• MyVariant Identifiers: chr2:g.157182708G>C (hg19) ; chr2:g.156326196G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326196G>C , CM000664.2:g.156326196G>C	GRCh38
NC_000002.11:g.157182708G>C , CM000664.1:g.157182708G>C	GRCh37
NC_000002.10:g.156890954G>C	NCBI36
NG_011821.1:g.11580C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1290C>G	ENSP00000514865.1:p.Ile430Met
ENST00000700229.1:c.458C>G
ENST00000700230.1:c.1034C>G	ENSP00000514867.1:n.1034C>G
ENST00000700231.1:c.1419C>G	ENSP00000514868.1:p.Ile473Met
ENST00000339562.9:c.1494C>G MANE Select	ENSP00000344479.4:p.Ile498Met
ENST00000675870.1:c.*5C>G	ENSP00000502739.1:n.*5C>G
ENST00000339562.8:c.1494C>G	ENSP00000344479.4:p.Ile498Met
ENST00000409108.6:c.1390C>G	ENSP00000386993.2:p.Arg464Gly
ENST00000409572.5:c.1494C>G	ENSP00000386747.1:p.Ile498Met
ENST00000417764.5:c.*5C>G	ENSP00000415632.1:n.*5C>G
ENST00000417972.5:c.*5C>G	ENSP00000394671.1:n.*5C>G
ENST00000426264.5:c.1305C>G	ENSP00000389986.1:p.Ile435Met
ENST00000429376.5:c.1201C>G	ENSP00000410952.1:p.Arg401Gly
NM_006186.3:c.1494C>G	NP_006177.1:p.Ile498Met
XM_005246621.2:c.1527C>G	XP_005246678.1:p.Ile509Met
XM_005246622.2:c.1305C>G	XP_005246679.1:p.Ile435Met
XM_005246623.1:c.1305C>G	XP_005246680.1:p.Ile435Met
XM_006712553.2:c.1452C>G	XP_006712616.1:p.Ile484Met
XM_011511246.1:c.1423C>G	XP_011509548.1:p.Arg475Gly
XR_427087.2:n.3579C>G
NM_173173.2:c.1305C>G	NP_775265.1:p.Ile435Met
XM_005246621.4:c.1527C>G	XP_005246678.1:p.Ile509Met
XM_006712553.4:c.1452C>G	XP_006712616.1:p.Ile484Met
XM_011511246.2:c.1423C>G	XP_011509548.1:p.Arg475Gly
XM_017004219.2:c.1494C>G	XP_016859708.1:p.Ile498Met
XM_017004220.2:c.1419C>G	XP_016859709.1:p.Ile473Met
XR_001738751.2:n.1741C>G
XR_001738752.2:n.1563C>G
XR_427087.4:n.1620C>G
NM_006186.4:c.1494C>G MANE Select	NP_006177.1:p.Ile498Met
NM_173173.3:c.1305C>G	NP_775265.1:p.Ile435Met