Canonical Allele Identifier: CA970507595
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs1894622266

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998183A>C , CM000677.2:g.60998183A>C GRCh38
NC_000015.9:g.61290382A>C , CM000677.1:g.61290382A>C GRCh37
NC_000015.8:g.59077674A>C NCBI36
NG_029246.1:g.236121T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230870T>G MANE Select ENSP00000335087.6:n.166+230870T>G
ENST00000335670.10:c.166+230870T>G ENSP00000335087.6:n.166+230870T>G
ENST00000551975.5:c.81+230870T>G
ENST00000557822.5:n.191+230870T>G
ENST00000559145.1:n.173+230870T>G
ENST00000561093.1:n.179+230870T>G
NM_134261.2:c.166+230870T>G NP_599023.1:n.166+230870T>G
XM_011521876.1:c.34+17615T>G XP_011520178.1:n.34+17615T>G
XM_011521878.1:c.-328+230870T>G XP_011520180.1:n.-328+230870T>G
XM_011521878.2:c.-328+230870T>G XP_011520180.1:n.-328+230870T>G
NM_134261.3:c.166+230870T>G MANE Select NP_599023.1:n.166+230870T>G