Canonical Allele Identifier: CA2181374300
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60777792G= , CM000677.2:g.60777792G= GRCh38
NC_000015.9:g.61069991G= , CM000677.1:g.61069991G= GRCh37
NC_000015.8:g.58857283G= NCBI36
NG_029246.1:g.456512C=

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.167-99106C= MANE Select ENSP00000335087.6:n.167-99106C=
ENST00000335670.10:c.167-99106C= ENSP00000335087.6:n.167-99106C=
ENST00000551975.5:c.82-99106C=
ENST00000557822.5:n.192-99106C=
ENST00000559145.1:n.174-99106C=
ENST00000561093.1:n.180-99106C=
NM_134261.2:c.167-99106C= NP_599023.1:n.167-99106C=
XM_005254584.3:c.28+63278C= XP_005254641.1:n.28+63278C=
XM_011521876.1:c.35-99106C= XP_011520178.1:n.35-99106C=
XM_011521878.1:c.-327-99106C= XP_011520180.1:n.-327-99106C=
XM_005254584.5:c.28+63278C= XP_005254641.1:n.28+63278C=
XM_011521878.2:c.-327-99106C= XP_011520180.1:n.-327-99106C=
NM_134261.3:c.167-99106C= MANE Select NP_599023.1:n.167-99106C=