Canonical Allele Identifier: CA2181533094
Community Standard Title: NM_134261.3(RORA):c.166+122143C=
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61106910G= , CM000677.2:g.61106910G= GRCh38
NC_000015.9:g.61399109G= , CM000677.1:g.61399109G= GRCh37
NC_000015.8:g.59186401G= NCBI36
NG_029246.1:g.127394C=

Transcript Alleles

HGVS Amino-acid Change
NM_134261.3:c.166+122143C= MANE Select NP_599023.1:n.166+122143C=
ENST00000335670.11:c.166+122143C= MANE Select ENSP00000335087.6:n.166+122143C=
NM_134261.2:c.166+122143C= NP_599023.1:n.166+122143C=
ENST00000335670.10:c.166+122143C= ENSP00000335087.6:n.166+122143C=
ENST00000551975.5:c.81+122143C=
ENST00000557822.5:n.191+122143C=
ENST00000559145.1:n.173+122143C=
ENST00000560300.1:n.182-65776C=
ENST00000561093.1:n.179+122143C=
XM_011521878.1:c.-328+122143C= XP_011520180.1:n.-328+122143C=
XM_011521878.2:c.-328+122143C= XP_011520180.1:n.-328+122143C=
XR_002957760.1:n.7251-2682C=