Canonical Allele Identifier: CA970491621
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs754499

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60844006G>C , CM000677.2:g.60844006G>C GRCh38
NC_000015.9:g.61136205G>C , CM000677.1:g.61136205G>C GRCh37
NC_000015.8:g.58923497G>C NCBI36
NG_029246.1:g.390298C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.167-165320C>G MANE Select ENSP00000335087.6:n.167-165320C>G
ENST00000335670.10:c.167-165320C>G ENSP00000335087.6:n.167-165320C>G
ENST00000551975.5:c.82-165320C>G
ENST00000557822.5:n.192-165320C>G
ENST00000559145.1:n.174-165320C>G
ENST00000561093.1:n.180-165320C>G
NM_134261.2:c.167-165320C>G NP_599023.1:n.167-165320C>G
XM_011521876.1:c.35-165320C>G XP_011520178.1:n.35-165320C>G
XM_011521878.1:c.-327-165320C>G XP_011520180.1:n.-327-165320C>G
XM_005254584.5:c.-2909C>G XP_005254641.1:n.-2909C>G
XM_011521878.2:c.-327-165320C>G XP_011520180.1:n.-327-165320C>G
NM_134261.3:c.167-165320C>G MANE Select NP_599023.1:n.167-165320C>G