Canonical Allele Identifier: CA272215392

Gene: RORA

Linked Data

• dbSNP Id: rs1026055690
• gnomAD v3: 15-60998319-A-G
• gnomAD v4: 15-60998319-A-G
• MyVariant Identifiers: chr15:g.61290518A>G (hg19) ; chr15:g.60998319A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998319A>G , CM000677.2:g.60998319A>G	GRCh38
NC_000015.9:g.61290518A>G , CM000677.1:g.61290518A>G	GRCh37
NC_000015.8:g.59077810A>G	NCBI36
NG_029246.1:g.235985T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230734T>C MANE Select	ENSP00000335087.6:n.166+230734T>C
ENST00000335670.10:c.166+230734T>C	ENSP00000335087.6:n.166+230734T>C
ENST00000551975.5:c.81+230734T>C
ENST00000557822.5:n.191+230734T>C
ENST00000559145.1:n.173+230734T>C
ENST00000561093.1:n.179+230734T>C
NM_134261.2:c.166+230734T>C	NP_599023.1:n.166+230734T>C
XM_011521876.1:c.34+17479T>C	XP_011520178.1:n.34+17479T>C
XM_011521878.1:c.-328+230734T>C	XP_011520180.1:n.-328+230734T>C
XM_011521878.2:c.-328+230734T>C	XP_011520180.1:n.-328+230734T>C
NM_134261.3:c.166+230734T>C MANE Select	NP_599023.1:n.166+230734T>C