Canonical Allele Identifier: CA272233740

Gene: RORA

Linked Data

• dbSNP Id: rs893353571
• gnomAD v3: 15-61148381-T-G
• gnomAD v4: 15-61148381-T-G
• MyVariant Identifiers: chr15:g.61440580T>G (hg19) ; chr15:g.61148381T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148381T>G , CM000677.2:g.61148381T>G	GRCh38
NC_000015.9:g.61440580T>G , CM000677.1:g.61440580T>G	GRCh37
NC_000015.8:g.59227872T>G	NCBI36
NG_029246.1:g.85923A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80672A>C MANE Select	ENSP00000335087.6:n.166+80672A>C
ENST00000335670.10:c.166+80672A>C	ENSP00000335087.6:n.166+80672A>C
ENST00000551975.5:c.81+80672A>C
ENST00000557822.5:n.191+80672A>C
ENST00000559145.1:n.173+80672A>C
ENST00000560300.1:n.181+80672A>C
ENST00000561093.1:n.179+80672A>C
NM_134261.2:c.166+80672A>C	NP_599023.1:n.166+80672A>C
XM_011521878.1:c.-328+80672A>C	XP_011520180.1:n.-328+80672A>C
XM_011521878.2:c.-328+80672A>C	XP_011520180.1:n.-328+80672A>C
NM_134261.3:c.166+80672A>C MANE Select	NP_599023.1:n.166+80672A>C