Canonical Allele Identifier: CA2181553208

Gene: RORA

Linked Data

• dbSNP Id: rs2079369609

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148414G>C , CM000677.2:g.61148414G>C	GRCh38
NC_000015.9:g.61440613G>C , CM000677.1:g.61440613G>C	GRCh37
NC_000015.8:g.59227905G>C	NCBI36
NG_029246.1:g.85890C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80639C>G MANE Select	ENSP00000335087.6:n.166+80639C>G
ENST00000335670.10:c.166+80639C>G	ENSP00000335087.6:n.166+80639C>G
ENST00000551975.5:c.81+80639C>G
ENST00000557822.5:n.191+80639C>G
ENST00000559145.1:n.173+80639C>G
ENST00000560300.1:n.181+80639C>G
ENST00000561093.1:n.179+80639C>G
NM_134261.2:c.166+80639C>G	NP_599023.1:n.166+80639C>G
XM_011521878.1:c.-328+80639C>G	XP_011520180.1:n.-328+80639C>G
XM_011521878.2:c.-328+80639C>G	XP_011520180.1:n.-328+80639C>G
NM_134261.3:c.166+80639C>G MANE Select	NP_599023.1:n.166+80639C>G