Canonical Allele Identifier: CA714566442

Gene: RORA

Linked Data

• dbSNP Id: rs1421994963
• MyVariant Identifiers: chr15:g.61290117A>G (hg19) ; chr15:g.60997918A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60997918A>G , CM000677.2:g.60997918A>G	GRCh38
NC_000015.9:g.61290117A>G , CM000677.1:g.61290117A>G	GRCh37
NC_000015.8:g.59077409A>G	NCBI36
NG_029246.1:g.236386T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+231135T>C MANE Select	ENSP00000335087.6:n.166+231135T>C
ENST00000335670.10:c.166+231135T>C	ENSP00000335087.6:n.166+231135T>C
ENST00000551975.5:c.81+231135T>C
ENST00000557822.5:n.191+231135T>C
ENST00000559145.1:n.173+231135T>C
ENST00000561093.1:n.179+231135T>C
NM_134261.2:c.166+231135T>C	NP_599023.1:n.166+231135T>C
XM_011521876.1:c.34+17880T>C	XP_011520178.1:n.34+17880T>C
XM_011521878.1:c.-328+231135T>C	XP_011520180.1:n.-328+231135T>C
XM_011521878.2:c.-328+231135T>C	XP_011520180.1:n.-328+231135T>C
NM_134261.3:c.166+231135T>C MANE Select	NP_599023.1:n.166+231135T>C