Canonical Allele Identifier: CA272215376

Gene: RORA

Linked Data

• dbSNP Id: rs546441213
• gnomAD v3: 15-60998231-A-C
• gnomAD v4: 15-60998231-A-C
• MyVariant Identifiers: chr15:g.61290430A>C (hg19) ; chr15:g.60998231A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998231A>C , CM000677.2:g.60998231A>C	GRCh38
NC_000015.9:g.61290430A>C , CM000677.1:g.61290430A>C	GRCh37
NC_000015.8:g.59077722A>C	NCBI36
NG_029246.1:g.236073T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230822T>G MANE Select	ENSP00000335087.6:n.166+230822T>G
ENST00000335670.10:c.166+230822T>G	ENSP00000335087.6:n.166+230822T>G
ENST00000551975.5:c.81+230822T>G
ENST00000557822.5:n.191+230822T>G
ENST00000559145.1:n.173+230822T>G
ENST00000561093.1:n.179+230822T>G
NM_134261.2:c.166+230822T>G	NP_599023.1:n.166+230822T>G
XM_011521876.1:c.34+17567T>G	XP_011520178.1:n.34+17567T>G
XM_011521878.1:c.-328+230822T>G	XP_011520180.1:n.-328+230822T>G
XM_011521878.2:c.-328+230822T>G	XP_011520180.1:n.-328+230822T>G
NM_134261.3:c.166+230822T>G MANE Select	NP_599023.1:n.166+230822T>G