Canonical Allele Identifier: CA2181499471
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61037515G= , CM000677.2:g.61037515G= GRCh38
NC_000015.9:g.61329714G= , CM000677.1:g.61329714G= GRCh37
NC_000015.8:g.59117006G= NCBI36
NG_029246.1:g.196789C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+191538C= MANE Select ENSP00000335087.6:n.166+191538C=
ENST00000335670.10:c.166+191538C= ENSP00000335087.6:n.166+191538C=
ENST00000551975.5:c.81+191538C=
ENST00000557822.5:n.191+191538C=
ENST00000559145.1:n.173+191538C=
ENST00000561093.1:n.179+191538C=
NM_134261.2:c.166+191538C= NP_599023.1:n.166+191538C=
XM_011521878.1:c.-328+191538C= XP_011520180.1:n.-328+191538C=
XM_011521878.2:c.-328+191538C= XP_011520180.1:n.-328+191538C=
XR_001751773.2:n.2610C=
XR_001751776.2:n.1088+1522C=
XR_001751777.2:n.967-2589C=
XR_002957755.1:n.7635C=
XR_002957756.1:n.4586C=
XR_002957757.1:n.7635C=
XR_002957758.1:n.7635C=
XR_002957759.1:n.7635C=
XR_002957760.1:n.11232C=
XR_002957761.1:n.7635C=
NM_134261.3:c.166+191538C= MANE Select NP_599023.1:n.166+191538C=