Canonical Allele Identifier: CA2181434210
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60901968C= , CM000677.2:g.60901968C= GRCh38
NC_000015.9:g.61194167C= , CM000677.1:g.61194167C= GRCh37
NC_000015.8:g.58981459C= NCBI36
NG_029246.1:g.332336G=

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.167-223282G= MANE Select ENSP00000335087.6:n.167-223282G=
ENST00000335670.10:c.167-223282G= ENSP00000335087.6:n.167-223282G=
ENST00000551975.5:c.82-223282G=
ENST00000557822.5:n.192-223282G=
ENST00000559145.1:n.174-223282G=
ENST00000561093.1:n.180-223282G=
NM_134261.2:c.167-223282G= NP_599023.1:n.167-223282G=
XM_011521876.1:c.34+113830G= XP_011520178.1:n.34+113830G=
XM_011521878.1:c.-327-223282G= XP_011520180.1:n.-327-223282G=
XM_011521878.2:c.-327-223282G= XP_011520180.1:n.-327-223282G=
NM_134261.3:c.167-223282G= MANE Select NP_599023.1:n.167-223282G=