Canonical Allele Identifier: CA272215365

Gene: RORA

Linked Data

• dbSNP Id: rs966154864
• gnomAD v3: 15-60998151-C-A
• gnomAD v4: 15-60998151-C-A
• MyVariant Identifiers: chr15:g.61290350C>A (hg19) ; chr15:g.60998151C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998151C>A , CM000677.2:g.60998151C>A	GRCh38
NC_000015.9:g.61290350C>A , CM000677.1:g.61290350C>A	GRCh37
NC_000015.8:g.59077642C>A	NCBI36
NG_029246.1:g.236153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230902G>T MANE Select	ENSP00000335087.6:n.166+230902G>T
ENST00000335670.10:c.166+230902G>T	ENSP00000335087.6:n.166+230902G>T
ENST00000551975.5:c.81+230902G>T
ENST00000557822.5:n.191+230902G>T
ENST00000559145.1:n.173+230902G>T
ENST00000561093.1:n.179+230902G>T
NM_134261.2:c.166+230902G>T	NP_599023.1:n.166+230902G>T
XM_011521876.1:c.34+17647G>T	XP_011520178.1:n.34+17647G>T
XM_011521878.1:c.-328+230902G>T	XP_011520180.1:n.-328+230902G>T
XM_011521878.2:c.-328+230902G>T	XP_011520180.1:n.-328+230902G>T
NM_134261.3:c.166+230902G>T MANE Select	NP_599023.1:n.166+230902G>T