Canonical Allele Identifier: CA2181480913
Gene: RORA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998318C= , CM000677.2:g.60998318C= GRCh38
NC_000015.9:g.61290517C= , CM000677.1:g.61290517C= GRCh37
NC_000015.8:g.59077809C= NCBI36
NG_029246.1:g.235986G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230735G= MANE Select ENSP00000335087.6:n.166+230735G=
ENST00000335670.10:c.166+230735G= ENSP00000335087.6:n.166+230735G=
ENST00000551975.5:c.81+230735G=
ENST00000557822.5:n.191+230735G=
ENST00000559145.1:n.173+230735G=
ENST00000561093.1:n.179+230735G=
NM_134261.2:c.166+230735G= NP_599023.1:n.166+230735G=
XM_011521876.1:c.34+17480G= XP_011520178.1:n.34+17480G=
XM_011521878.1:c.-328+230735G= XP_011520180.1:n.-328+230735G=
XM_011521878.2:c.-328+230735G= XP_011520180.1:n.-328+230735G=
NM_134261.3:c.166+230735G= MANE Select NP_599023.1:n.166+230735G=
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