Canonical Allele Identifier: CA272220154

Gene: RORA

Linked Data

• dbSNP Id: rs186704157
• gnomAD v2: 15-61329741-C-T
• gnomAD v3: 15-61037542-C-T
• gnomAD v4: 15-61037542-C-T
• MyVariant Identifiers: chr15:g.61329741C>T (hg19) ; chr15:g.61037542C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037542C>T , CM000677.2:g.61037542C>T	GRCh38
NC_000015.9:g.61329741C>T , CM000677.1:g.61329741C>T	GRCh37
NC_000015.8:g.59117033C>T	NCBI36
NG_029246.1:g.196762G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191511G>A MANE Select	ENSP00000335087.6:n.166+191511G>A
ENST00000335670.10:c.166+191511G>A	ENSP00000335087.6:n.166+191511G>A
ENST00000551975.5:c.81+191511G>A
ENST00000557822.5:n.191+191511G>A
ENST00000559145.1:n.173+191511G>A
ENST00000561093.1:n.179+191511G>A
NM_134261.2:c.166+191511G>A	NP_599023.1:n.166+191511G>A
XM_011521878.1:c.-328+191511G>A	XP_011520180.1:n.-328+191511G>A
XM_011521878.2:c.-328+191511G>A	XP_011520180.1:n.-328+191511G>A
XR_001751773.2:n.2583G>A
XR_001751776.2:n.1088+1495G>A
XR_001751777.2:n.967-2616G>A
XR_002957755.1:n.7608G>A
XR_002957756.1:n.4559G>A
XR_002957757.1:n.7608G>A
XR_002957758.1:n.7608G>A
XR_002957759.1:n.7608G>A
XR_002957760.1:n.11205G>A
XR_002957761.1:n.7608G>A
NM_134261.3:c.166+191511G>A MANE Select	NP_599023.1:n.166+191511G>A