Canonical Allele Identifier: CA970501432

Gene: RORA

Linked Data

• dbSNP Id: rs2072061731
• gnomAD v3: 15-60770780-G-A
• gnomAD v4: 15-60770780-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60770780G>A , CM000677.2:g.60770780G>A	GRCh38
NC_000015.9:g.61062979G>A , CM000677.1:g.61062979G>A	GRCh37
NC_000015.8:g.58850271G>A	NCBI36
NG_029246.1:g.463524C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-92094C>T MANE Select	ENSP00000335087.6:n.167-92094C>T
ENST00000335670.10:c.167-92094C>T	ENSP00000335087.6:n.167-92094C>T
ENST00000551975.5:c.82-92094C>T
ENST00000557822.5:n.192-92094C>T
ENST00000559145.1:n.174-92094C>T
ENST00000561093.1:n.180-92094C>T
NM_134261.2:c.167-92094C>T	NP_599023.1:n.167-92094C>T
XM_005254584.3:c.28+70290C>T	XP_005254641.1:n.28+70290C>T
XM_011521876.1:c.35-92094C>T	XP_011520178.1:n.35-92094C>T
XM_011521878.1:c.-327-92094C>T	XP_011520180.1:n.-327-92094C>T
XM_005254584.5:c.28+70290C>T	XP_005254641.1:n.28+70290C>T
XM_011521878.2:c.-327-92094C>T	XP_011520180.1:n.-327-92094C>T
NM_134261.3:c.167-92094C>T MANE Select	NP_599023.1:n.167-92094C>T