Canonical Allele Identifier: CA272188108

Gene: RORA

Linked Data

• dbSNP Id: rs910144098
• gnomAD v3: 15-60777828-G-C
• gnomAD v4: 15-60777828-G-C
• MyVariant Identifiers: chr15:g.61070027G>C (hg19) ; chr15:g.60777828G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60777828G>C , CM000677.2:g.60777828G>C	GRCh38
NC_000015.9:g.61070027G>C , CM000677.1:g.61070027G>C	GRCh37
NC_000015.8:g.58857319G>C	NCBI36
NG_029246.1:g.456476C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.167-99142C>G MANE Select	ENSP00000335087.6:n.167-99142C>G
ENST00000335670.10:c.167-99142C>G	ENSP00000335087.6:n.167-99142C>G
ENST00000551975.5:c.82-99142C>G
ENST00000557822.5:n.192-99142C>G
ENST00000559145.1:n.174-99142C>G
ENST00000561093.1:n.180-99142C>G
NM_134261.2:c.167-99142C>G	NP_599023.1:n.167-99142C>G
XM_005254584.3:c.28+63242C>G	XP_005254641.1:n.28+63242C>G
XM_011521876.1:c.35-99142C>G	XP_011520178.1:n.35-99142C>G
XM_011521878.1:c.-327-99142C>G	XP_011520180.1:n.-327-99142C>G
XM_005254584.5:c.28+63242C>G	XP_005254641.1:n.28+63242C>G
XM_011521878.2:c.-327-99142C>G	XP_011520180.1:n.-327-99142C>G
NM_134261.3:c.167-99142C>G MANE Select	NP_599023.1:n.167-99142C>G