Canonical Allele Identifier: CA2181480776
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998000T= , CM000677.2:g.60998000T= GRCh38
NC_000015.9:g.61290199T= , CM000677.1:g.61290199T= GRCh37
NC_000015.8:g.59077491T= NCBI36
NG_029246.1:g.236304A=

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+231053A= MANE Select ENSP00000335087.6:n.166+231053A=
ENST00000335670.10:c.166+231053A= ENSP00000335087.6:n.166+231053A=
ENST00000551975.5:c.81+231053A=
ENST00000557822.5:n.191+231053A=
ENST00000559145.1:n.173+231053A=
ENST00000561093.1:n.179+231053A=
NM_134261.2:c.166+231053A= NP_599023.1:n.166+231053A=
XM_011521876.1:c.34+17798A= XP_011520178.1:n.34+17798A=
XM_011521878.1:c.-328+231053A= XP_011520180.1:n.-328+231053A=
XM_011521878.2:c.-328+231053A= XP_011520180.1:n.-328+231053A=
NM_134261.3:c.166+231053A= MANE Select NP_599023.1:n.166+231053A=