Canonical Allele Identifier: CA14199189
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs12912233

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60974897C>T , CM000677.2:g.60974897C>T GRCh38
NC_000015.9:g.61267096C>T , CM000677.1:g.61267096C>T GRCh37
NC_000015.8:g.59054388C>T NCBI36
NG_029246.1:g.259407G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+254156G>A MANE Select ENSP00000335087.6:n.166+254156G>A
ENST00000335670.10:c.166+254156G>A ENSP00000335087.6:n.166+254156G>A
ENST00000551975.5:c.81+254156G>A
ENST00000557822.5:n.191+254156G>A
ENST00000559145.1:n.173+254156G>A
ENST00000561093.1:n.179+254156G>A
NM_134261.2:c.166+254156G>A NP_599023.1:n.166+254156G>A
XM_011521876.1:c.34+40901G>A XP_011520178.1:n.34+40901G>A
XM_011521878.1:c.-328+254156G>A XP_011520180.1:n.-328+254156G>A
XM_011521878.2:c.-328+254156G>A XP_011520180.1:n.-328+254156G>A
NM_134261.3:c.166+254156G>A MANE Select NP_599023.1:n.166+254156G>A