Canonical Allele Identifier: CA348683372
Gene: NR4A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156330165A>G , CM000664.2:g.156330165A>G GRCh38
NC_000002.11:g.157186677A>G , CM000664.1:g.157186677A>G GRCh37
NC_000002.10:g.156894923A>G NCBI36
NG_011821.1:g.7611T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000421709.2:c.-13-155T>C ENSP00000388120.2:n.-13-155T>C
ENST00000700228.1:c.-108T>C ENSP00000514865.1:n.-108T>C
ENST00000700231.1:c.22T>C ENSP00000514868.1:p.Tyr8His
ENST00000339562.9:c.22T>C MANE Select ENSP00000344479.4:p.Tyr8His
ENST00000675870.1:c.-13-155T>C ENSP00000502739.1:n.-13-155T>C
ENST00000339562.8:c.22T>C ENSP00000344479.4:p.Tyr8His
ENST00000409108.6:c.22T>C ENSP00000386993.2:p.Tyr8His
ENST00000409572.5:c.22T>C ENSP00000386747.1:p.Tyr8His
ENST00000417764.5:c.-13-155T>C ENSP00000415632.1:n.-13-155T>C
ENST00000417972.5:c.-13-155T>C ENSP00000394671.1:n.-13-155T>C
ENST00000421709.1:c.-13-155T>C ENSP00000388120.1:n.-13-155T>C
ENST00000424077.1:c.22T>C ENSP00000406808.1:p.Tyr8His
ENST00000426264.5:c.-13-155T>C ENSP00000389986.1:n.-13-155T>C
ENST00000429376.5:c.-13-155T>C ENSP00000410952.1:n.-13-155T>C
NM_006186.3:c.22T>C NP_006177.1:p.Tyr8His
XM_005246621.2:c.55T>C XP_005246678.1:p.Tyr19His
XM_005246622.2:c.-13-155T>C XP_005246679.1:n.-13-155T>C
XM_005246623.1:c.-13-155T>C XP_005246680.1:n.-13-155T>C
XM_006712553.2:c.55T>C XP_006712616.1:p.Tyr19His
XM_011511246.1:c.55T>C XP_011509548.1:p.Tyr19His
XR_427087.2:n.2228T>C
NM_173173.2:c.-13-155T>C NP_775265.1:n.-13-155T>C
XM_005246621.4:c.55T>C XP_005246678.1:p.Tyr19His
XM_006712553.4:c.55T>C XP_006712616.1:p.Tyr19His
XM_011511246.2:c.55T>C XP_011509548.1:p.Tyr19His
XM_017004219.2:c.22T>C XP_016859708.1:p.Tyr8His
XM_017004220.2:c.22T>C XP_016859709.1:p.Tyr8His
XR_001738751.2:n.390T>C
XR_001738752.2:n.367-155T>C
XR_427087.4:n.269T>C
NM_006186.4:c.22T>C MANE Select NP_006177.1:p.Tyr8His
NM_173173.3:c.-13-155T>C NP_775265.1:n.-13-155T>C