Canonical Allele Identifier: CA2181553242
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs2079370356
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61148499G>C , CM000677.2:g.61148499G>C GRCh38
NC_000015.9:g.61440698G>C , CM000677.1:g.61440698G>C GRCh37
NC_000015.8:g.59227990G>C NCBI36
NG_029246.1:g.85805C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+80554C>G MANE Select ENSP00000335087.6:n.166+80554C>G
ENST00000335670.10:c.166+80554C>G ENSP00000335087.6:n.166+80554C>G
ENST00000551975.5:c.81+80554C>G
ENST00000557822.5:n.191+80554C>G
ENST00000559145.1:n.173+80554C>G
ENST00000560300.1:n.181+80554C>G
ENST00000561093.1:n.179+80554C>G
NM_134261.2:c.166+80554C>G NP_599023.1:n.166+80554C>G
XM_011521878.1:c.-328+80554C>G XP_011520180.1:n.-328+80554C>G
XM_011521878.2:c.-328+80554C>G XP_011520180.1:n.-328+80554C>G
NM_134261.3:c.166+80554C>G MANE Select NP_599023.1:n.166+80554C>G
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