Canonical Allele Identifier: CA970507560
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs1894613595

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60997972A>G , CM000677.2:g.60997972A>G GRCh38
NC_000015.9:g.61290171A>G , CM000677.1:g.61290171A>G GRCh37
NC_000015.8:g.59077463A>G NCBI36
NG_029246.1:g.236332T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+231081T>C MANE Select ENSP00000335087.6:n.166+231081T>C
ENST00000335670.10:c.166+231081T>C ENSP00000335087.6:n.166+231081T>C
ENST00000551975.5:c.81+231081T>C
ENST00000557822.5:n.191+231081T>C
ENST00000559145.1:n.173+231081T>C
ENST00000561093.1:n.179+231081T>C
NM_134261.2:c.166+231081T>C NP_599023.1:n.166+231081T>C
XM_011521876.1:c.34+17826T>C XP_011520178.1:n.34+17826T>C
XM_011521878.1:c.-328+231081T>C XP_011520180.1:n.-328+231081T>C
XM_011521878.2:c.-328+231081T>C XP_011520180.1:n.-328+231081T>C
NM_134261.3:c.166+231081T>C MANE Select NP_599023.1:n.166+231081T>C