Canonical Allele Identifier: CA970530550
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs2079369637

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61148416C>A , CM000677.2:g.61148416C>A GRCh38
NC_000015.9:g.61440615C>A , CM000677.1:g.61440615C>A GRCh37
NC_000015.8:g.59227907C>A NCBI36
NG_029246.1:g.85888G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+80637G>T MANE Select ENSP00000335087.6:n.166+80637G>T
ENST00000335670.10:c.166+80637G>T ENSP00000335087.6:n.166+80637G>T
ENST00000551975.5:c.81+80637G>T
ENST00000557822.5:n.191+80637G>T
ENST00000559145.1:n.173+80637G>T
ENST00000560300.1:n.181+80637G>T
ENST00000561093.1:n.179+80637G>T
NM_134261.2:c.166+80637G>T NP_599023.1:n.166+80637G>T
XM_011521878.1:c.-328+80637G>T XP_011520180.1:n.-328+80637G>T
XM_011521878.2:c.-328+80637G>T XP_011520180.1:n.-328+80637G>T
NM_134261.3:c.166+80637G>T MANE Select NP_599023.1:n.166+80637G>T