Canonical Allele Identifier: CA1916416
Gene: NR4A2 HGNC NCBI

Linked Data

dbSNP Id: rs370355149

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156329577G>T , CM000664.2:g.156329577G>T GRCh38
NC_000002.11:g.157186089G>T , CM000664.1:g.157186089G>T GRCh37
NC_000002.10:g.156894335G>T NCBI36
NG_011821.1:g.8199C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.421C>A ENSP00000388120.2:p.Pro141Thr
ENST00000700228.1:c.481C>A ENSP00000514865.1:p.Pro161Thr
ENST00000700230.1:c.43C>A ENSP00000514867.1:p.Pro15Thr
ENST00000700231.1:c.610C>A ENSP00000514868.1:p.Pro204Thr
ENST00000339562.9:c.610C>A MANE Select ENSP00000344479.4:p.Pro204Thr
ENST00000675870.1:c.421C>A ENSP00000502739.1:p.Pro141Thr
ENST00000339562.8:c.610C>A ENSP00000344479.4:p.Pro204Thr
ENST00000406048.2:c.208+337C>A
ENST00000409108.6:c.610C>A ENSP00000386993.2:p.Pro204Thr
ENST00000409572.5:c.610C>A ENSP00000386747.1:p.Pro204Thr
ENST00000417764.5:c.421C>A ENSP00000415632.1:p.Pro141Thr
ENST00000417972.5:c.421C>A ENSP00000394671.1:p.Pro141Thr
ENST00000424077.1:c.610C>A ENSP00000406808.1:p.Pro204Thr
ENST00000426264.5:c.421C>A ENSP00000389986.1:p.Pro141Thr
ENST00000429376.5:c.421C>A ENSP00000410952.1:p.Pro141Thr
NM_006186.3:c.610C>A NP_006177.1:p.Pro204Thr
XM_005246621.2:c.643C>A XP_005246678.1:p.Pro215Thr
XM_005246622.2:c.421C>A XP_005246679.1:p.Pro141Thr
XM_005246623.1:c.421C>A XP_005246680.1:p.Pro141Thr
XM_006712553.2:c.643C>A XP_006712616.1:p.Pro215Thr
XM_011511246.1:c.643C>A XP_011509548.1:p.Pro215Thr
XR_427087.2:n.2816C>A
NM_173173.2:c.421C>A NP_775265.1:p.Pro141Thr
XM_005246621.4:c.643C>A XP_005246678.1:p.Pro215Thr
XM_006712553.4:c.643C>A XP_006712616.1:p.Pro215Thr
XM_011511246.2:c.643C>A XP_011509548.1:p.Pro215Thr
XM_017004219.2:c.610C>A XP_016859708.1:p.Pro204Thr
XM_017004220.2:c.610C>A XP_016859709.1:p.Pro204Thr
XR_001738751.2:n.978C>A
XR_001738752.2:n.800C>A
XR_427087.4:n.857C>A
NM_006186.4:c.610C>A MANE Select NP_006177.1:p.Pro204Thr
NM_173173.3:c.421C>A NP_775265.1:p.Pro141Thr