Canonical Allele Identifier: CA272233750

Gene: RORA

Linked Data

• dbSNP Id: rs974005943
• MyVariant Identifiers: chr15:g.61440713A>G (hg19) ; chr15:g.61148514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148514A>G , CM000677.2:g.61148514A>G	GRCh38
NC_000015.9:g.61440713A>G , CM000677.1:g.61440713A>G	GRCh37
NC_000015.8:g.59228005A>G	NCBI36
NG_029246.1:g.85790T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80539T>C MANE Select	ENSP00000335087.6:n.166+80539T>C
ENST00000335670.10:c.166+80539T>C	ENSP00000335087.6:n.166+80539T>C
ENST00000551975.5:c.81+80539T>C
ENST00000557822.5:n.191+80539T>C
ENST00000559145.1:n.173+80539T>C
ENST00000560300.1:n.181+80539T>C
ENST00000561093.1:n.179+80539T>C
NM_134261.2:c.166+80539T>C	NP_599023.1:n.166+80539T>C
XM_011521878.1:c.-328+80539T>C	XP_011520180.1:n.-328+80539T>C
XM_011521878.2:c.-328+80539T>C	XP_011520180.1:n.-328+80539T>C
NM_134261.3:c.166+80539T>C MANE Select	NP_599023.1:n.166+80539T>C