Canonical Allele Identifier: CA714566524

Gene: RORA

Linked Data

• dbSNP Id: rs1174247773
• MyVariant Identifiers: chr15:g.61290208G>T (hg19) ; chr15:g.60998009G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998009G>T , CM000677.2:g.60998009G>T	GRCh38
NC_000015.9:g.61290208G>T , CM000677.1:g.61290208G>T	GRCh37
NC_000015.8:g.59077500G>T	NCBI36
NG_029246.1:g.236295C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+231044C>A MANE Select	ENSP00000335087.6:n.166+231044C>A
ENST00000335670.10:c.166+231044C>A	ENSP00000335087.6:n.166+231044C>A
ENST00000551975.5:c.81+231044C>A
ENST00000557822.5:n.191+231044C>A
ENST00000559145.1:n.173+231044C>A
ENST00000561093.1:n.179+231044C>A
NM_134261.2:c.166+231044C>A	NP_599023.1:n.166+231044C>A
XM_011521876.1:c.34+17789C>A	XP_011520178.1:n.34+17789C>A
XM_011521878.1:c.-328+231044C>A	XP_011520180.1:n.-328+231044C>A
XM_011521878.2:c.-328+231044C>A	XP_011520180.1:n.-328+231044C>A
NM_134261.3:c.166+231044C>A MANE Select	NP_599023.1:n.166+231044C>A