Canonical Allele Identifier: CA2181480908
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs1894627544

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998310T>G , CM000677.2:g.60998310T>G GRCh38
NC_000015.9:g.61290509T>G , CM000677.1:g.61290509T>G GRCh37
NC_000015.8:g.59077801T>G NCBI36
NG_029246.1:g.235994A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230743A>C MANE Select ENSP00000335087.6:n.166+230743A>C
ENST00000335670.10:c.166+230743A>C ENSP00000335087.6:n.166+230743A>C
ENST00000551975.5:c.81+230743A>C
ENST00000557822.5:n.191+230743A>C
ENST00000559145.1:n.173+230743A>C
ENST00000561093.1:n.179+230743A>C
NM_134261.2:c.166+230743A>C NP_599023.1:n.166+230743A>C
XM_011521876.1:c.34+17488A>C XP_011520178.1:n.34+17488A>C
XM_011521878.1:c.-328+230743A>C XP_011520180.1:n.-328+230743A>C
XM_011521878.2:c.-328+230743A>C XP_011520180.1:n.-328+230743A>C
NM_134261.3:c.166+230743A>C MANE Select NP_599023.1:n.166+230743A>C