Canonical Allele Identifier: CA2804400767
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61148280G>A , CM000677.2:g.61148280G>A GRCh38
NC_000015.9:g.61440479G>A , CM000677.1:g.61440479G>A GRCh37
NC_000015.8:g.59227771G>A NCBI36
NG_029246.1:g.86024C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+80773C>T MANE Select ENSP00000335087.6:n.166+80773C>T
ENST00000335670.10:c.166+80773C>T ENSP00000335087.6:n.166+80773C>T
ENST00000551975.5:c.81+80773C>T
ENST00000557822.5:n.191+80773C>T
ENST00000559145.1:n.173+80773C>T
ENST00000560300.1:n.181+80773C>T
ENST00000561093.1:n.179+80773C>T
NM_134261.2:c.166+80773C>T NP_599023.1:n.166+80773C>T
XM_011521878.1:c.-328+80773C>T XP_011520180.1:n.-328+80773C>T
XM_011521878.2:c.-328+80773C>T XP_011520180.1:n.-328+80773C>T
NM_134261.3:c.166+80773C>T MANE Select NP_599023.1:n.166+80773C>T