Canonical Allele Identifier: CA714590634

Gene: RORA

Linked Data

• dbSNP Id: rs1253754427
• MyVariant Identifiers: chr15:g.61329876G>A (hg19) ; chr15:g.61037677G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037677G>A , CM000677.2:g.61037677G>A	GRCh38
NC_000015.9:g.61329876G>A , CM000677.1:g.61329876G>A	GRCh37
NC_000015.8:g.59117168G>A	NCBI36
NG_029246.1:g.196627C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191376C>T MANE Select	ENSP00000335087.6:n.166+191376C>T
ENST00000335670.10:c.166+191376C>T	ENSP00000335087.6:n.166+191376C>T
ENST00000551975.5:c.81+191376C>T
ENST00000557822.5:n.191+191376C>T
ENST00000559145.1:n.173+191376C>T
ENST00000561093.1:n.179+191376C>T
NM_134261.2:c.166+191376C>T	NP_599023.1:n.166+191376C>T
XM_011521878.1:c.-328+191376C>T	XP_011520180.1:n.-328+191376C>T
XM_011521878.2:c.-328+191376C>T	XP_011520180.1:n.-328+191376C>T
XR_001751773.2:n.2448C>T
XR_001751776.2:n.1088+1360C>T
XR_001751777.2:n.967-2751C>T
XR_002957755.1:n.7473C>T
XR_002957756.1:n.4424C>T
XR_002957757.1:n.7473C>T
XR_002957758.1:n.7473C>T
XR_002957759.1:n.7473C>T
XR_002957760.1:n.11070C>T
XR_002957761.1:n.7473C>T
NM_134261.3:c.166+191376C>T MANE Select	NP_599023.1:n.166+191376C>T