Canonical Allele Identifier: CA714600772

Gene: RORA

Linked Data

• dbSNP Id: rs1450534642
• gnomAD v3: 15-61148512-A-G
• gnomAD v4: 15-61148512-A-G
• MyVariant Identifiers: chr15:g.61440711A>G (hg19) ; chr15:g.61148512A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148512A>G , CM000677.2:g.61148512A>G	GRCh38
NC_000015.9:g.61440711A>G , CM000677.1:g.61440711A>G	GRCh37
NC_000015.8:g.59228003A>G	NCBI36
NG_029246.1:g.85792T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+80541T>C MANE Select	ENSP00000335087.6:n.166+80541T>C
ENST00000335670.10:c.166+80541T>C	ENSP00000335087.6:n.166+80541T>C
ENST00000551975.5:c.81+80541T>C
ENST00000557822.5:n.191+80541T>C
ENST00000559145.1:n.173+80541T>C
ENST00000560300.1:n.181+80541T>C
ENST00000561093.1:n.179+80541T>C
NM_134261.2:c.166+80541T>C	NP_599023.1:n.166+80541T>C
XM_011521878.1:c.-328+80541T>C	XP_011520180.1:n.-328+80541T>C
XM_011521878.2:c.-328+80541T>C	XP_011520180.1:n.-328+80541T>C
NM_134261.3:c.166+80541T>C MANE Select	NP_599023.1:n.166+80541T>C