Canonical Allele Identifier: CA2181480791
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998042C= , CM000677.2:g.60998042C= GRCh38
NC_000015.9:g.61290241C= , CM000677.1:g.61290241C= GRCh37
NC_000015.8:g.59077533C= NCBI36
NG_029246.1:g.236262G=

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+231011G= MANE Select ENSP00000335087.6:n.166+231011G=
ENST00000335670.10:c.166+231011G= ENSP00000335087.6:n.166+231011G=
ENST00000551975.5:c.81+231011G=
ENST00000557822.5:n.191+231011G=
ENST00000559145.1:n.173+231011G=
ENST00000561093.1:n.179+231011G=
NM_134261.2:c.166+231011G= NP_599023.1:n.166+231011G=
XM_011521876.1:c.34+17756G= XP_011520178.1:n.34+17756G=
XM_011521878.1:c.-328+231011G= XP_011520180.1:n.-328+231011G=
XM_011521878.2:c.-328+231011G= XP_011520180.1:n.-328+231011G=
NM_134261.3:c.166+231011G= MANE Select NP_599023.1:n.166+231011G=