Canonical Allele Identifier: CA272203546

Gene: RORA

Linked Data

• dbSNP Id: rs185958863
• gnomAD v3: 15-60901967-C-G
• gnomAD v4: 15-60901967-C-G
• MyVariant Identifiers: chr15:g.61194166C>G (hg19) ; chr15:g.60901967C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60901967C>G , CM000677.2:g.60901967C>G	GRCh38
NC_000015.9:g.61194166C>G , CM000677.1:g.61194166C>G	GRCh37
NC_000015.8:g.58981458C>G	NCBI36
NG_029246.1:g.332337G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.167-223281G>C MANE Select	ENSP00000335087.6:n.167-223281G>C
ENST00000335670.10:c.167-223281G>C	ENSP00000335087.6:n.167-223281G>C
ENST00000551975.5:c.82-223281G>C
ENST00000557822.5:n.192-223281G>C
ENST00000559145.1:n.174-223281G>C
ENST00000561093.1:n.180-223281G>C
NM_134261.2:c.167-223281G>C	NP_599023.1:n.167-223281G>C
XM_011521876.1:c.34+113831G>C	XP_011520178.1:n.34+113831G>C
XM_011521878.1:c.-327-223281G>C	XP_011520180.1:n.-327-223281G>C
XM_011521878.2:c.-327-223281G>C	XP_011520180.1:n.-327-223281G>C
NM_134261.3:c.167-223281G>C MANE Select	NP_599023.1:n.167-223281G>C