Canonical Allele Identifier: CA2181480746
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs1595868824

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60997943C>A , CM000677.2:g.60997943C>A GRCh38
NC_000015.9:g.61290142C>A , CM000677.1:g.61290142C>A GRCh37
NC_000015.8:g.59077434C>A NCBI36
NG_029246.1:g.236361G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+231110G>T MANE Select ENSP00000335087.6:n.166+231110G>T
ENST00000335670.10:c.166+231110G>T ENSP00000335087.6:n.166+231110G>T
ENST00000551975.5:c.81+231110G>T
ENST00000557822.5:n.191+231110G>T
ENST00000559145.1:n.173+231110G>T
ENST00000561093.1:n.179+231110G>T
NM_134261.2:c.166+231110G>T NP_599023.1:n.166+231110G>T
XM_011521876.1:c.34+17855G>T XP_011520178.1:n.34+17855G>T
XM_011521878.1:c.-328+231110G>T XP_011520180.1:n.-328+231110G>T
XM_011521878.2:c.-328+231110G>T XP_011520180.1:n.-328+231110G>T
NM_134261.3:c.166+231110G>T MANE Select NP_599023.1:n.166+231110G>T