Canonical Allele Identifier: CA714590657

Gene: RORA

Linked Data

• dbSNP Id: rs1267127535
• gnomAD v3: 15-61037717-T-C
• gnomAD v4: 15-61037717-T-C
• MyVariant Identifiers: chr15:g.61329916T>C (hg19) ; chr15:g.61037717T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037717T>C , CM000677.2:g.61037717T>C	GRCh38
NC_000015.9:g.61329916T>C , CM000677.1:g.61329916T>C	GRCh37
NC_000015.8:g.59117208T>C	NCBI36
NG_029246.1:g.196587A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191336A>G MANE Select	ENSP00000335087.6:n.166+191336A>G
ENST00000335670.10:c.166+191336A>G	ENSP00000335087.6:n.166+191336A>G
ENST00000551975.5:c.81+191336A>G
ENST00000557822.5:n.191+191336A>G
ENST00000559145.1:n.173+191336A>G
ENST00000561093.1:n.179+191336A>G
NM_134261.2:c.166+191336A>G	NP_599023.1:n.166+191336A>G
XM_011521878.1:c.-328+191336A>G	XP_011520180.1:n.-328+191336A>G
XM_011521878.2:c.-328+191336A>G	XP_011520180.1:n.-328+191336A>G
XR_001751773.2:n.2408A>G
XR_001751776.2:n.1088+1320A>G
XR_001751777.2:n.967-2791A>G
XR_002957755.1:n.7433A>G
XR_002957756.1:n.4384A>G
XR_002957757.1:n.7433A>G
XR_002957758.1:n.7433A>G
XR_002957759.1:n.7433A>G
XR_002957760.1:n.11030A>G
XR_002957761.1:n.7433A>G
NM_134261.3:c.166+191336A>G MANE Select	NP_599023.1:n.166+191336A>G