Canonical Allele Identifier: CA2181480858
Gene: RORA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998190T= , CM000677.2:g.60998190T= GRCh38
NC_000015.9:g.61290389T= , CM000677.1:g.61290389T= GRCh37
NC_000015.8:g.59077681T= NCBI36
NG_029246.1:g.236114A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230863A= MANE Select ENSP00000335087.6:n.166+230863A=
ENST00000335670.10:c.166+230863A= ENSP00000335087.6:n.166+230863A=
ENST00000551975.5:c.81+230863A=
ENST00000557822.5:n.191+230863A=
ENST00000559145.1:n.173+230863A=
ENST00000561093.1:n.179+230863A=
NM_134261.2:c.166+230863A= NP_599023.1:n.166+230863A=
XM_011521876.1:c.34+17608A= XP_011520178.1:n.34+17608A=
XM_011521878.1:c.-328+230863A= XP_011520180.1:n.-328+230863A=
XM_011521878.2:c.-328+230863A= XP_011520180.1:n.-328+230863A=
NM_134261.3:c.166+230863A= MANE Select NP_599023.1:n.166+230863A=
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