Canonical Allele Identifier: CA2181434213
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60901973A= , CM000677.2:g.60901973A= GRCh38
NC_000015.9:g.61194172A= , CM000677.1:g.61194172A= GRCh37
NC_000015.8:g.58981464A= NCBI36
NG_029246.1:g.332331T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.167-223287T= MANE Select ENSP00000335087.6:n.167-223287T=
ENST00000335670.10:c.167-223287T= ENSP00000335087.6:n.167-223287T=
ENST00000551975.5:c.82-223287T=
ENST00000557822.5:n.192-223287T=
ENST00000559145.1:n.174-223287T=
ENST00000561093.1:n.180-223287T=
NM_134261.2:c.167-223287T= NP_599023.1:n.167-223287T=
XM_011521876.1:c.34+113825T= XP_011520178.1:n.34+113825T=
XM_011521878.1:c.-327-223287T= XP_011520180.1:n.-327-223287T=
XM_011521878.2:c.-327-223287T= XP_011520180.1:n.-327-223287T=
NM_134261.3:c.167-223287T= MANE Select NP_599023.1:n.167-223287T=