Canonical Allele Identifier: CA714590613

Gene: RORA

Linked Data

• dbSNP Id: rs1411548196
• MyVariant Identifiers: chr15:g.61329850C>T (hg19) ; chr15:g.61037651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037651C>T , CM000677.2:g.61037651C>T	GRCh38
NC_000015.9:g.61329850C>T , CM000677.1:g.61329850C>T	GRCh37
NC_000015.8:g.59117142C>T	NCBI36
NG_029246.1:g.196653G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191402G>A MANE Select	ENSP00000335087.6:n.166+191402G>A
ENST00000335670.10:c.166+191402G>A	ENSP00000335087.6:n.166+191402G>A
ENST00000551975.5:c.81+191402G>A
ENST00000557822.5:n.191+191402G>A
ENST00000559145.1:n.173+191402G>A
ENST00000561093.1:n.179+191402G>A
NM_134261.2:c.166+191402G>A	NP_599023.1:n.166+191402G>A
XM_011521878.1:c.-328+191402G>A	XP_011520180.1:n.-328+191402G>A
XM_011521878.2:c.-328+191402G>A	XP_011520180.1:n.-328+191402G>A
XR_001751773.2:n.2474G>A
XR_001751776.2:n.1088+1386G>A
XR_001751777.2:n.967-2725G>A
XR_002957755.1:n.7499G>A
XR_002957756.1:n.4450G>A
XR_002957757.1:n.7499G>A
XR_002957758.1:n.7499G>A
XR_002957759.1:n.7499G>A
XR_002957760.1:n.11096G>A
XR_002957761.1:n.7499G>A
NM_134261.3:c.166+191402G>A MANE Select	NP_599023.1:n.166+191402G>A