Canonical Allele Identifier: CA2181553166
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs2079368774
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61148314T>G , CM000677.2:g.61148314T>G GRCh38
NC_000015.9:g.61440513T>G , CM000677.1:g.61440513T>G GRCh37
NC_000015.8:g.59227805T>G NCBI36
NG_029246.1:g.85990A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+80739A>C MANE Select ENSP00000335087.6:n.166+80739A>C
ENST00000335670.10:c.166+80739A>C ENSP00000335087.6:n.166+80739A>C
ENST00000551975.5:c.81+80739A>C
ENST00000557822.5:n.191+80739A>C
ENST00000559145.1:n.173+80739A>C
ENST00000560300.1:n.181+80739A>C
ENST00000561093.1:n.179+80739A>C
NM_134261.2:c.166+80739A>C NP_599023.1:n.166+80739A>C
XM_011521878.1:c.-328+80739A>C XP_011520180.1:n.-328+80739A>C
XM_011521878.2:c.-328+80739A>C XP_011520180.1:n.-328+80739A>C
NM_134261.3:c.166+80739A>C MANE Select NP_599023.1:n.166+80739A>C
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