Canonical Allele Identifier: CA2181371036

Gene: RORA

Linked Data

• dbSNP Id: rs2072061623
• gnomAD v3: 15-60770776-C-T
• gnomAD v4: 15-60770776-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60770776C>T , CM000677.2:g.60770776C>T	GRCh38
NC_000015.9:g.61062975C>T , CM000677.1:g.61062975C>T	GRCh37
NC_000015.8:g.58850267C>T	NCBI36
NG_029246.1:g.463528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-92090G>A MANE Select	ENSP00000335087.6:n.167-92090G>A
ENST00000335670.10:c.167-92090G>A	ENSP00000335087.6:n.167-92090G>A
ENST00000551975.5:c.82-92090G>A
ENST00000557822.5:n.192-92090G>A
ENST00000559145.1:n.174-92090G>A
ENST00000561093.1:n.180-92090G>A
NM_134261.2:c.167-92090G>A	NP_599023.1:n.167-92090G>A
XM_005254584.3:c.28+70294G>A	XP_005254641.1:n.28+70294G>A
XM_011521876.1:c.35-92090G>A	XP_011520178.1:n.35-92090G>A
XM_011521878.1:c.-327-92090G>A	XP_011520180.1:n.-327-92090G>A
XM_005254584.5:c.28+70294G>A	XP_005254641.1:n.28+70294G>A
XM_011521878.2:c.-327-92090G>A	XP_011520180.1:n.-327-92090G>A
NM_134261.3:c.167-92090G>A MANE Select	NP_599023.1:n.167-92090G>A