Canonical Allele Identifier: CA272220170

Gene: RORA

Linked Data

• dbSNP Id: rs989644643
• gnomAD v2: 15-61329837-C-G
• gnomAD v3: 15-61037638-C-G
• gnomAD v4: 15-61037638-C-G
• MyVariant Identifiers: chr15:g.61329837C>G (hg19) ; chr15:g.61037638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037638C>G , CM000677.2:g.61037638C>G	GRCh38
NC_000015.9:g.61329837C>G , CM000677.1:g.61329837C>G	GRCh37
NC_000015.8:g.59117129C>G	NCBI36
NG_029246.1:g.196666G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191415G>C MANE Select	ENSP00000335087.6:n.166+191415G>C
ENST00000335670.10:c.166+191415G>C	ENSP00000335087.6:n.166+191415G>C
ENST00000551975.5:c.81+191415G>C
ENST00000557822.5:n.191+191415G>C
ENST00000559145.1:n.173+191415G>C
ENST00000561093.1:n.179+191415G>C
NM_134261.2:c.166+191415G>C	NP_599023.1:n.166+191415G>C
XM_011521878.1:c.-328+191415G>C	XP_011520180.1:n.-328+191415G>C
XM_011521878.2:c.-328+191415G>C	XP_011520180.1:n.-328+191415G>C
XR_001751773.2:n.2487G>C
XR_001751776.2:n.1088+1399G>C
XR_001751777.2:n.967-2712G>C
XR_002957755.1:n.7512G>C
XR_002957756.1:n.4463G>C
XR_002957757.1:n.7512G>C
XR_002957758.1:n.7512G>C
XR_002957759.1:n.7512G>C
XR_002957760.1:n.11109G>C
XR_002957761.1:n.7512G>C
NM_134261.3:c.166+191415G>C MANE Select	NP_599023.1:n.166+191415G>C