Canonical Allele Identifier: CA2181480927
Gene: RORA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998345G= , CM000677.2:g.60998345G= GRCh38
NC_000015.9:g.61290544G= , CM000677.1:g.61290544G= GRCh37
NC_000015.8:g.59077836G= NCBI36
NG_029246.1:g.235959C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230708C= MANE Select ENSP00000335087.6:n.166+230708C=
ENST00000335670.10:c.166+230708C= ENSP00000335087.6:n.166+230708C=
ENST00000551975.5:c.81+230708C=
ENST00000557822.5:n.191+230708C=
ENST00000559145.1:n.173+230708C=
ENST00000561093.1:n.179+230708C=
NM_134261.2:c.166+230708C= NP_599023.1:n.166+230708C=
XM_011521876.1:c.34+17453C= XP_011520178.1:n.34+17453C=
XM_011521878.1:c.-328+230708C= XP_011520180.1:n.-328+230708C=
XM_011521878.2:c.-328+230708C= XP_011520180.1:n.-328+230708C=
NM_134261.3:c.166+230708C= MANE Select NP_599023.1:n.166+230708C=
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