Canonical Allele Identifier: CA970507607
Gene: RORA HGNC NCBI

Linked Data

gnomAD v3: 15-60998231-A-T
gnomAD v4: 15-60998231-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998231A>T , CM000677.2:g.60998231A>T GRCh38
NC_000015.9:g.61290430A>T , CM000677.1:g.61290430A>T GRCh37
NC_000015.8:g.59077722A>T NCBI36
NG_029246.1:g.236073T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230822T>A MANE Select ENSP00000335087.6:n.166+230822T>A
ENST00000335670.10:c.166+230822T>A ENSP00000335087.6:n.166+230822T>A
ENST00000551975.5:c.81+230822T>A
ENST00000557822.5:n.191+230822T>A
ENST00000559145.1:n.173+230822T>A
ENST00000561093.1:n.179+230822T>A
NM_134261.2:c.166+230822T>A NP_599023.1:n.166+230822T>A
XM_011521876.1:c.34+17567T>A XP_011520178.1:n.34+17567T>A
XM_011521878.1:c.-328+230822T>A XP_011520180.1:n.-328+230822T>A
XM_011521878.2:c.-328+230822T>A XP_011520180.1:n.-328+230822T>A
NM_134261.3:c.166+230822T>A MANE Select NP_599023.1:n.166+230822T>A
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