Canonical Allele Identifier: CA618468781

Gene: RORA

Linked Data

• dbSNP Id: rs1365688610
• gnomAD v2: 15-61194192-G-T
• gnomAD v3: 15-60901993-G-T
• gnomAD v4: 15-60901993-G-T
• MyVariant Identifiers: chr15:g.61194192G>T (hg19) ; chr15:g.60901993G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60901993G>T , CM000677.2:g.60901993G>T	GRCh38
NC_000015.9:g.61194192G>T , CM000677.1:g.61194192G>T	GRCh37
NC_000015.8:g.58981484G>T	NCBI36
NG_029246.1:g.332311C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-223307C>A MANE Select	ENSP00000335087.6:n.167-223307C>A
ENST00000335670.10:c.167-223307C>A	ENSP00000335087.6:n.167-223307C>A
ENST00000551975.5:c.82-223307C>A
ENST00000557822.5:n.192-223307C>A
ENST00000559145.1:n.174-223307C>A
ENST00000561093.1:n.180-223307C>A
NM_134261.2:c.167-223307C>A	NP_599023.1:n.167-223307C>A
XM_011521876.1:c.34+113805C>A	XP_011520178.1:n.34+113805C>A
XM_011521878.1:c.-327-223307C>A	XP_011520180.1:n.-327-223307C>A
XM_011521878.2:c.-327-223307C>A	XP_011520180.1:n.-327-223307C>A
NM_134261.3:c.167-223307C>A MANE Select	NP_599023.1:n.167-223307C>A