Canonical Allele Identifier: CA272220171

Gene: RORA

Linked Data

• dbSNP Id: rs931272965
• MyVariant Identifiers: chr15:g.61329842A>G (hg19) ; chr15:g.61037643A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037643A>G , CM000677.2:g.61037643A>G	GRCh38
NC_000015.9:g.61329842A>G , CM000677.1:g.61329842A>G	GRCh37
NC_000015.8:g.59117134A>G	NCBI36
NG_029246.1:g.196661T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191410T>C MANE Select	ENSP00000335087.6:n.166+191410T>C
ENST00000335670.10:c.166+191410T>C	ENSP00000335087.6:n.166+191410T>C
ENST00000551975.5:c.81+191410T>C
ENST00000557822.5:n.191+191410T>C
ENST00000559145.1:n.173+191410T>C
ENST00000561093.1:n.179+191410T>C
NM_134261.2:c.166+191410T>C	NP_599023.1:n.166+191410T>C
XM_011521878.1:c.-328+191410T>C	XP_011520180.1:n.-328+191410T>C
XM_011521878.2:c.-328+191410T>C	XP_011520180.1:n.-328+191410T>C
XR_001751773.2:n.2482T>C
XR_001751776.2:n.1088+1394T>C
XR_001751777.2:n.967-2717T>C
XR_002957755.1:n.7507T>C
XR_002957756.1:n.4458T>C
XR_002957757.1:n.7507T>C
XR_002957758.1:n.7507T>C
XR_002957759.1:n.7507T>C
XR_002957760.1:n.11104T>C
XR_002957761.1:n.7507T>C
NM_134261.3:c.166+191410T>C MANE Select	NP_599023.1:n.166+191410T>C