Canonical Allele Identifier: CA2181480857

Gene: RORA

Linked Data

• dbSNP Id: rs1894622656

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998189G>T , CM000677.2:g.60998189G>T	GRCh38
NC_000015.9:g.61290388G>T , CM000677.1:g.61290388G>T	GRCh37
NC_000015.8:g.59077680G>T	NCBI36
NG_029246.1:g.236115C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230864C>A MANE Select	ENSP00000335087.6:n.166+230864C>A
ENST00000335670.10:c.166+230864C>A	ENSP00000335087.6:n.166+230864C>A
ENST00000551975.5:c.81+230864C>A
ENST00000557822.5:n.191+230864C>A
ENST00000559145.1:n.173+230864C>A
ENST00000561093.1:n.179+230864C>A
NM_134261.2:c.166+230864C>A	NP_599023.1:n.166+230864C>A
XM_011521876.1:c.34+17609C>A	XP_011520178.1:n.34+17609C>A
XM_011521878.1:c.-328+230864C>A	XP_011520180.1:n.-328+230864C>A
XM_011521878.2:c.-328+230864C>A	XP_011520180.1:n.-328+230864C>A
NM_134261.3:c.166+230864C>A MANE Select	NP_599023.1:n.166+230864C>A