Canonical Allele Identifier: CA2580581810
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60777789C>G , CM000677.2:g.60777789C>G GRCh38
NC_000015.9:g.61069988C>G , CM000677.1:g.61069988C>G GRCh37
NC_000015.8:g.58857280C>G NCBI36
NG_029246.1:g.456515G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.167-99103G>C MANE Select ENSP00000335087.6:n.167-99103G>C
ENST00000335670.10:c.167-99103G>C ENSP00000335087.6:n.167-99103G>C
ENST00000551975.5:c.82-99103G>C
ENST00000557822.5:n.192-99103G>C
ENST00000559145.1:n.174-99103G>C
ENST00000561093.1:n.180-99103G>C
NM_134261.2:c.167-99103G>C NP_599023.1:n.167-99103G>C
XM_005254584.3:c.28+63281G>C XP_005254641.1:n.28+63281G>C
XM_011521876.1:c.35-99103G>C XP_011520178.1:n.35-99103G>C
XM_011521878.1:c.-327-99103G>C XP_011520180.1:n.-327-99103G>C
XM_005254584.5:c.28+63281G>C XP_005254641.1:n.28+63281G>C
XM_011521878.2:c.-327-99103G>C XP_011520180.1:n.-327-99103G>C
NM_134261.3:c.167-99103G>C MANE Select NP_599023.1:n.167-99103G>C