Canonical Allele Identifier: CA348681894

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329498-A-G
• MyVariant Identifiers: chr2:g.157186010A>G (hg19) ; chr2:g.156329498A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329498A>G , CM000664.2:g.156329498A>G	GRCh38
NC_000002.11:g.157186010A>G , CM000664.1:g.157186010A>G	GRCh37
NC_000002.10:g.156894256A>G	NCBI36
NG_011821.1:g.8278T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.560T>C	ENSP00000514865.1:p.Met187Thr
ENST00000700230.1:c.122T>C	ENSP00000514867.1:p.Met41Thr
ENST00000700231.1:c.689T>C	ENSP00000514868.1:p.Met230Thr
ENST00000339562.9:c.689T>C MANE Select	ENSP00000344479.4:p.Met230Thr
ENST00000675870.1:c.500T>C	ENSP00000502739.1:p.Met167Thr
ENST00000339562.8:c.689T>C	ENSP00000344479.4:p.Met230Thr
ENST00000406048.2:c.208+416T>C
ENST00000409108.6:c.689T>C	ENSP00000386993.2:p.Met230Thr
ENST00000409572.5:c.689T>C	ENSP00000386747.1:p.Met230Thr
ENST00000417764.5:c.500T>C	ENSP00000415632.1:p.Met167Thr
ENST00000417972.5:c.500T>C	ENSP00000394671.1:p.Met167Thr
ENST00000424077.1:c.689T>C	ENSP00000406808.1:p.Met230Thr
ENST00000426264.5:c.500T>C	ENSP00000389986.1:p.Met167Thr
ENST00000429376.5:c.500T>C	ENSP00000410952.1:p.Met167Thr
NM_006186.3:c.689T>C	NP_006177.1:p.Met230Thr
XM_005246621.2:c.722T>C	XP_005246678.1:p.Met241Thr
XM_005246622.2:c.500T>C	XP_005246679.1:p.Met167Thr
XM_005246623.1:c.500T>C	XP_005246680.1:p.Met167Thr
XM_006712553.2:c.722T>C	XP_006712616.1:p.Met241Thr
XM_011511246.1:c.722T>C	XP_011509548.1:p.Met241Thr
XR_427087.2:n.2895T>C
NM_173173.2:c.500T>C	NP_775265.1:p.Met167Thr
XM_005246621.4:c.722T>C	XP_005246678.1:p.Met241Thr
XM_006712553.4:c.722T>C	XP_006712616.1:p.Met241Thr
XM_011511246.2:c.722T>C	XP_011509548.1:p.Met241Thr
XM_017004219.2:c.689T>C	XP_016859708.1:p.Met230Thr
XM_017004220.2:c.689T>C	XP_016859709.1:p.Met230Thr
XR_001738751.2:n.1057T>C
XR_001738752.2:n.879T>C
XR_427087.4:n.936T>C
NM_006186.4:c.689T>C MANE Select	NP_006177.1:p.Met230Thr
NM_173173.3:c.500T>C	NP_775265.1:p.Met167Thr