Canonical Allele Identifier: CA272220152

Gene: RORA

Linked Data

• dbSNP Id: rs998045042
• gnomAD v2: 15-61329738-G-T
• gnomAD v3: 15-61037539-G-T
• gnomAD v4: 15-61037539-G-T
• MyVariant Identifiers: chr15:g.61329738G>T (hg19) ; chr15:g.61037539G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037539G>T , CM000677.2:g.61037539G>T	GRCh38
NC_000015.9:g.61329738G>T , CM000677.1:g.61329738G>T	GRCh37
NC_000015.8:g.59117030G>T	NCBI36
NG_029246.1:g.196765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191514C>A MANE Select	ENSP00000335087.6:n.166+191514C>A
ENST00000335670.10:c.166+191514C>A	ENSP00000335087.6:n.166+191514C>A
ENST00000551975.5:c.81+191514C>A
ENST00000557822.5:n.191+191514C>A
ENST00000559145.1:n.173+191514C>A
ENST00000561093.1:n.179+191514C>A
NM_134261.2:c.166+191514C>A	NP_599023.1:n.166+191514C>A
XM_011521878.1:c.-328+191514C>A	XP_011520180.1:n.-328+191514C>A
XM_011521878.2:c.-328+191514C>A	XP_011520180.1:n.-328+191514C>A
XR_001751773.2:n.2586C>A
XR_001751776.2:n.1088+1498C>A
XR_001751777.2:n.967-2613C>A
XR_002957755.1:n.7611C>A
XR_002957756.1:n.4562C>A
XR_002957757.1:n.7611C>A
XR_002957758.1:n.7611C>A
XR_002957759.1:n.7611C>A
XR_002957760.1:n.11208C>A
XR_002957761.1:n.7611C>A
NM_134261.3:c.166+191514C>A MANE Select	NP_599023.1:n.166+191514C>A