Canonical Allele Identifier: CA2181480889
Gene: RORA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998264G= , CM000677.2:g.60998264G= GRCh38
NC_000015.9:g.61290463G= , CM000677.1:g.61290463G= GRCh37
NC_000015.8:g.59077755G= NCBI36
NG_029246.1:g.236040C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230789C= MANE Select ENSP00000335087.6:n.166+230789C=
ENST00000335670.10:c.166+230789C= ENSP00000335087.6:n.166+230789C=
ENST00000551975.5:c.81+230789C=
ENST00000557822.5:n.191+230789C=
ENST00000559145.1:n.173+230789C=
ENST00000561093.1:n.179+230789C=
NM_134261.2:c.166+230789C= NP_599023.1:n.166+230789C=
XM_011521876.1:c.34+17534C= XP_011520178.1:n.34+17534C=
XM_011521878.1:c.-328+230789C= XP_011520180.1:n.-328+230789C=
XM_011521878.2:c.-328+230789C= XP_011520180.1:n.-328+230789C=
NM_134261.3:c.166+230789C= MANE Select NP_599023.1:n.166+230789C=
Search 100 bp 5'
Search 100 bp 3'