Canonical Allele Identifier: CA272233738

Gene: RORA

Linked Data

• dbSNP Id: rs921519055
• gnomAD v2: 15-61440573-G-A
• gnomAD v3: 15-61148374-G-A
• gnomAD v4: 15-61148374-G-A
• MyVariant Identifiers: chr15:g.61440573G>A (hg19) ; chr15:g.61148374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148374G>A , CM000677.2:g.61148374G>A	GRCh38
NC_000015.9:g.61440573G>A , CM000677.1:g.61440573G>A	GRCh37
NC_000015.8:g.59227865G>A	NCBI36
NG_029246.1:g.85930C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80679C>T MANE Select	ENSP00000335087.6:n.166+80679C>T
ENST00000335670.10:c.166+80679C>T	ENSP00000335087.6:n.166+80679C>T
ENST00000551975.5:c.81+80679C>T
ENST00000557822.5:n.191+80679C>T
ENST00000559145.1:n.173+80679C>T
ENST00000560300.1:n.181+80679C>T
ENST00000561093.1:n.179+80679C>T
NM_134261.2:c.166+80679C>T	NP_599023.1:n.166+80679C>T
XM_011521878.1:c.-328+80679C>T	XP_011520180.1:n.-328+80679C>T
XM_011521878.2:c.-328+80679C>T	XP_011520180.1:n.-328+80679C>T
NM_134261.3:c.166+80679C>T MANE Select	NP_599023.1:n.166+80679C>T