Canonical Allele Identifier: CA714566543

Gene: RORA

Linked Data

• dbSNP Id: rs1488688788
• gnomAD v3: 15-60998047-G-C
• gnomAD v4: 15-60998047-G-C
• MyVariant Identifiers: chr15:g.61290246G>C (hg19) ; chr15:g.60998047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998047G>C , CM000677.2:g.60998047G>C	GRCh38
NC_000015.9:g.61290246G>C , CM000677.1:g.61290246G>C	GRCh37
NC_000015.8:g.59077538G>C	NCBI36
NG_029246.1:g.236257C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+231006C>G MANE Select	ENSP00000335087.6:n.166+231006C>G
ENST00000335670.10:c.166+231006C>G	ENSP00000335087.6:n.166+231006C>G
ENST00000551975.5:c.81+231006C>G
ENST00000557822.5:n.191+231006C>G
ENST00000559145.1:n.173+231006C>G
ENST00000561093.1:n.179+231006C>G
NM_134261.2:c.166+231006C>G	NP_599023.1:n.166+231006C>G
XM_011521876.1:c.34+17751C>G	XP_011520178.1:n.34+17751C>G
XM_011521878.1:c.-328+231006C>G	XP_011520180.1:n.-328+231006C>G
XM_011521878.2:c.-328+231006C>G	XP_011520180.1:n.-328+231006C>G
NM_134261.3:c.166+231006C>G MANE Select	NP_599023.1:n.166+231006C>G