Canonical Allele Identifier: CA714550598

Gene: RORA

Linked Data

• dbSNP Id: rs1262133610
• gnomAD v3: 15-60777697-G-A
• gnomAD v4: 15-60777697-G-A
• MyVariant Identifiers: chr15:g.61069896G>A (hg19) ; chr15:g.60777697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60777697G>A , CM000677.2:g.60777697G>A	GRCh38
NC_000015.9:g.61069896G>A , CM000677.1:g.61069896G>A	GRCh37
NC_000015.8:g.58857188G>A	NCBI36
NG_029246.1:g.456607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-99011C>T MANE Select	ENSP00000335087.6:n.167-99011C>T
ENST00000335670.10:c.167-99011C>T	ENSP00000335087.6:n.167-99011C>T
ENST00000551975.5:c.82-99011C>T
ENST00000557822.5:n.192-99011C>T
ENST00000559145.1:n.174-99011C>T
ENST00000561093.1:n.180-99011C>T
NM_134261.2:c.167-99011C>T	NP_599023.1:n.167-99011C>T
XM_005254584.3:c.28+63373C>T	XP_005254641.1:n.28+63373C>T
XM_011521876.1:c.35-99011C>T	XP_011520178.1:n.35-99011C>T
XM_011521878.1:c.-327-99011C>T	XP_011520180.1:n.-327-99011C>T
XM_005254584.5:c.28+63373C>T	XP_005254641.1:n.28+63373C>T
XM_011521878.2:c.-327-99011C>T	XP_011520180.1:n.-327-99011C>T
NM_134261.3:c.167-99011C>T MANE Select	NP_599023.1:n.167-99011C>T