Canonical Allele Identifier: CA714600785

Gene: RORA

Linked Data

• dbSNP Id: rs1219639957
• MyVariant Identifiers: chr15:g.61440737C>T (hg19) ; chr15:g.61148538C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148538C>T , CM000677.2:g.61148538C>T	GRCh38
NC_000015.9:g.61440737C>T , CM000677.1:g.61440737C>T	GRCh37
NC_000015.8:g.59228029C>T	NCBI36
NG_029246.1:g.85766G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80515G>A MANE Select	ENSP00000335087.6:n.166+80515G>A
ENST00000335670.10:c.166+80515G>A	ENSP00000335087.6:n.166+80515G>A
ENST00000551975.5:c.81+80515G>A
ENST00000557822.5:n.191+80515G>A
ENST00000559145.1:n.173+80515G>A
ENST00000560300.1:n.181+80515G>A
ENST00000561093.1:n.179+80515G>A
NM_134261.2:c.166+80515G>A	NP_599023.1:n.166+80515G>A
XM_011521878.1:c.-328+80515G>A	XP_011520180.1:n.-328+80515G>A
XM_011521878.2:c.-328+80515G>A	XP_011520180.1:n.-328+80515G>A
NM_134261.3:c.166+80515G>A MANE Select	NP_599023.1:n.166+80515G>A