Canonical Allele Identifier: CA2181553240

Gene: RORA

Linked Data

• dbSNP Id: rs2079370327

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148494C>A , CM000677.2:g.61148494C>A	GRCh38
NC_000015.9:g.61440693C>A , CM000677.1:g.61440693C>A	GRCh37
NC_000015.8:g.59227985C>A	NCBI36
NG_029246.1:g.85810G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80559G>T MANE Select	ENSP00000335087.6:n.166+80559G>T
ENST00000335670.10:c.166+80559G>T	ENSP00000335087.6:n.166+80559G>T
ENST00000551975.5:c.81+80559G>T
ENST00000557822.5:n.191+80559G>T
ENST00000559145.1:n.173+80559G>T
ENST00000560300.1:n.181+80559G>T
ENST00000561093.1:n.179+80559G>T
NM_134261.2:c.166+80559G>T	NP_599023.1:n.166+80559G>T
XM_011521878.1:c.-328+80559G>T	XP_011520180.1:n.-328+80559G>T
XM_011521878.2:c.-328+80559G>T	XP_011520180.1:n.-328+80559G>T
NM_134261.3:c.166+80559G>T MANE Select	NP_599023.1:n.166+80559G>T