Canonical Allele Identifier: CA2181553205

Gene: RORA

Linked Data

• dbSNP Id: rs2079369555

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148404A>G , CM000677.2:g.61148404A>G	GRCh38
NC_000015.9:g.61440603A>G , CM000677.1:g.61440603A>G	GRCh37
NC_000015.8:g.59227895A>G	NCBI36
NG_029246.1:g.85900T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80649T>C MANE Select	ENSP00000335087.6:n.166+80649T>C
ENST00000335670.10:c.166+80649T>C	ENSP00000335087.6:n.166+80649T>C
ENST00000551975.5:c.81+80649T>C
ENST00000557822.5:n.191+80649T>C
ENST00000559145.1:n.173+80649T>C
ENST00000560300.1:n.181+80649T>C
ENST00000561093.1:n.179+80649T>C
NM_134261.2:c.166+80649T>C	NP_599023.1:n.166+80649T>C
XM_011521878.1:c.-328+80649T>C	XP_011520180.1:n.-328+80649T>C
XM_011521878.2:c.-328+80649T>C	XP_011520180.1:n.-328+80649T>C
NM_134261.3:c.166+80649T>C MANE Select	NP_599023.1:n.166+80649T>C