Canonical Allele Identifier: CA14133576
Gene: RORA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10519097

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60997989C>T , CM000677.2:g.60997989C>T GRCh38
NC_000015.8:g.59077480C>T NCBI36
NC_000015.9:g.61290188C>T , CM000677.1:g.61290188C>T GRCh37
NG_029246.1:g.236315G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.10:c.166+231064G>A ENSP00000335087.6:p.=
ENST00000551975.5:n.81+231064G>A
ENST00000557822.5:n.191+231064G>A
ENST00000559145.1:n.173+231064G>A
ENST00000561093.1:n.179+231064G>A
NM_134261.2:c.166+231064G>A VV NP_599023.1:p.=
XM_011521876.1:c.34+17809G>A XP_011520178.1:p.=
XM_011521878.1:c.-328+231064G>A XP_011520180.1:p.=