Canonical Allele Identifier: CA618479145

Gene: RORA

Linked Data

• dbSNP Id: rs1185959453
• gnomAD v2: 15-61329692-C-A
• gnomAD v3: 15-61037493-C-A
• gnomAD v4: 15-61037493-C-A
• MyVariant Identifiers: chr15:g.61329692C>A (hg19) ; chr15:g.61037493C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037493C>A , CM000677.2:g.61037493C>A	GRCh38
NC_000015.9:g.61329692C>A , CM000677.1:g.61329692C>A	GRCh37
NC_000015.8:g.59116984C>A	NCBI36
NG_029246.1:g.196811G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+191560G>T MANE Select	ENSP00000335087.6:n.166+191560G>T
ENST00000335670.10:c.166+191560G>T	ENSP00000335087.6:n.166+191560G>T
ENST00000551975.5:c.81+191560G>T
ENST00000557822.5:n.191+191560G>T
ENST00000559145.1:n.173+191560G>T
ENST00000561093.1:n.179+191560G>T
NM_134261.2:c.166+191560G>T	NP_599023.1:n.166+191560G>T
XM_011521878.1:c.-328+191560G>T	XP_011520180.1:n.-328+191560G>T
XM_011521878.2:c.-328+191560G>T	XP_011520180.1:n.-328+191560G>T
XR_001751773.2:n.2632G>T
XR_001751776.2:n.1088+1544G>T
XR_001751777.2:n.967-2567G>T
XR_002957755.1:n.7657G>T
XR_002957756.1:n.4608G>T
XR_002957757.1:n.7657G>T
XR_002957758.1:n.7657G>T
XR_002957759.1:n.7657G>T
XR_002957760.1:n.11254G>T
XR_002957761.1:n.7657G>T
NM_134261.3:c.166+191560G>T MANE Select	NP_599023.1:n.166+191560G>T