Canonical Allele Identifier: CA2181553159
Gene: RORA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61148306G= , CM000677.2:g.61148306G= GRCh38
NC_000015.9:g.61440505G= , CM000677.1:g.61440505G= GRCh37
NC_000015.8:g.59227797G= NCBI36
NG_029246.1:g.85998C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+80747C= MANE Select ENSP00000335087.6:n.166+80747C=
ENST00000335670.10:c.166+80747C= ENSP00000335087.6:n.166+80747C=
ENST00000551975.5:c.81+80747C=
ENST00000557822.5:n.191+80747C=
ENST00000559145.1:n.173+80747C=
ENST00000560300.1:n.181+80747C=
ENST00000561093.1:n.179+80747C=
NM_134261.2:c.166+80747C= NP_599023.1:n.166+80747C=
XM_011521878.1:c.-328+80747C= XP_011520180.1:n.-328+80747C=
XM_011521878.2:c.-328+80747C= XP_011520180.1:n.-328+80747C=
NM_134261.3:c.166+80747C= MANE Select NP_599023.1:n.166+80747C=
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