Canonical Allele Identifier: CA272215355

Gene: RORA

Linked Data

• dbSNP Id: rs76437176
• gnomAD v2: 15-61290251-C-T
• gnomAD v3: 15-60998052-C-T
• gnomAD v4: 15-60998052-C-T
• MyVariant Identifiers: chr15:g.61290251C>T (hg19) ; chr15:g.60998052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998052C>T , CM000677.2:g.60998052C>T	GRCh38
NC_000015.9:g.61290251C>T , CM000677.1:g.61290251C>T	GRCh37
NC_000015.8:g.59077543C>T	NCBI36
NG_029246.1:g.236252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+231001G>A MANE Select	ENSP00000335087.6:n.166+231001G>A
ENST00000335670.10:c.166+231001G>A	ENSP00000335087.6:n.166+231001G>A
ENST00000551975.5:c.81+231001G>A
ENST00000557822.5:n.191+231001G>A
ENST00000559145.1:n.173+231001G>A
ENST00000561093.1:n.179+231001G>A
NM_134261.2:c.166+231001G>A	NP_599023.1:n.166+231001G>A
XM_011521876.1:c.34+17746G>A	XP_011520178.1:n.34+17746G>A
XM_011521878.1:c.-328+231001G>A	XP_011520180.1:n.-328+231001G>A
XM_011521878.2:c.-328+231001G>A	XP_011520180.1:n.-328+231001G>A
NM_134261.3:c.166+231001G>A MANE Select	NP_599023.1:n.166+231001G>A