Canonical Allele Identifier: CA2181411756
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60855305T>G , CM000677.2:g.60855305T>G GRCh38
NC_000015.9:g.61147504T>G , CM000677.1:g.61147504T>G GRCh37
NC_000015.8:g.58934796T>G NCBI36
NG_029246.1:g.378999A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.167-176619A>C MANE Select ENSP00000335087.6:n.167-176619A>C
ENST00000335670.10:c.167-176619A>C ENSP00000335087.6:n.167-176619A>C
ENST00000551975.5:c.82-176619A>C
ENST00000557822.5:n.192-176619A>C
ENST00000559145.1:n.174-176619A>C
ENST00000561093.1:n.180-176619A>C
NM_134261.2:c.167-176619A>C NP_599023.1:n.167-176619A>C
XM_011521876.1:c.34+160493A>C XP_011520178.1:n.34+160493A>C
XM_011521878.1:c.-327-176619A>C XP_011520180.1:n.-327-176619A>C
XM_011521878.2:c.-327-176619A>C XP_011520180.1:n.-327-176619A>C
NM_134261.3:c.167-176619A>C MANE Select NP_599023.1:n.167-176619A>C