Canonical Allele Identifier: CA272215385

Gene: RORA

Linked Data

• dbSNP Id: rs145116538
• gnomAD v2: 15-61290496-G-C
• gnomAD v3: 15-60998297-G-C
• gnomAD v4: 15-60998297-G-C
• MyVariant Identifiers: chr15:g.61290496G>C (hg19) ; chr15:g.60998297G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998297G>C , CM000677.2:g.60998297G>C	GRCh38
NC_000015.9:g.61290496G>C , CM000677.1:g.61290496G>C	GRCh37
NC_000015.8:g.59077788G>C	NCBI36
NG_029246.1:g.236007C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230756C>G MANE Select	ENSP00000335087.6:n.166+230756C>G
ENST00000335670.10:c.166+230756C>G	ENSP00000335087.6:n.166+230756C>G
ENST00000551975.5:c.81+230756C>G
ENST00000557822.5:n.191+230756C>G
ENST00000559145.1:n.173+230756C>G
ENST00000561093.1:n.179+230756C>G
NM_134261.2:c.166+230756C>G	NP_599023.1:n.166+230756C>G
XM_011521876.1:c.34+17501C>G	XP_011520178.1:n.34+17501C>G
XM_011521878.1:c.-328+230756C>G	XP_011520180.1:n.-328+230756C>G
XM_011521878.2:c.-328+230756C>G	XP_011520180.1:n.-328+230756C>G
NM_134261.3:c.166+230756C>G MANE Select	NP_599023.1:n.166+230756C>G