Canonical Allele Identifier: CA970507571
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs1894615388
gnomAD v3: 15-60998016-A-T
gnomAD v4: 15-60998016-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998016A>T , CM000677.2:g.60998016A>T GRCh38
NC_000015.9:g.61290215A>T , CM000677.1:g.61290215A>T GRCh37
NC_000015.8:g.59077507A>T NCBI36
NG_029246.1:g.236288T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+231037T>A MANE Select ENSP00000335087.6:n.166+231037T>A
ENST00000335670.10:c.166+231037T>A ENSP00000335087.6:n.166+231037T>A
ENST00000551975.5:c.81+231037T>A
ENST00000557822.5:n.191+231037T>A
ENST00000559145.1:n.173+231037T>A
ENST00000561093.1:n.179+231037T>A
NM_134261.2:c.166+231037T>A NP_599023.1:n.166+231037T>A
XM_011521876.1:c.34+17782T>A XP_011520178.1:n.34+17782T>A
XM_011521878.1:c.-328+231037T>A XP_011520180.1:n.-328+231037T>A
XM_011521878.2:c.-328+231037T>A XP_011520180.1:n.-328+231037T>A
NM_134261.3:c.166+231037T>A MANE Select NP_599023.1:n.166+231037T>A
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