Canonical Allele Identifier: CA2181480784
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs1894615501
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998020C>T , CM000677.2:g.60998020C>T GRCh38
NC_000015.9:g.61290219C>T , CM000677.1:g.61290219C>T GRCh37
NC_000015.8:g.59077511C>T NCBI36
NG_029246.1:g.236284G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+231033G>A MANE Select ENSP00000335087.6:n.166+231033G>A
ENST00000335670.10:c.166+231033G>A ENSP00000335087.6:n.166+231033G>A
ENST00000551975.5:c.81+231033G>A
ENST00000557822.5:n.191+231033G>A
ENST00000559145.1:n.173+231033G>A
ENST00000561093.1:n.179+231033G>A
NM_134261.2:c.166+231033G>A NP_599023.1:n.166+231033G>A
XM_011521876.1:c.34+17778G>A XP_011520178.1:n.34+17778G>A
XM_011521878.1:c.-328+231033G>A XP_011520180.1:n.-328+231033G>A
XM_011521878.2:c.-328+231033G>A XP_011520180.1:n.-328+231033G>A
NM_134261.3:c.166+231033G>A MANE Select NP_599023.1:n.166+231033G>A
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