Canonical Allele Identifier: CA2664797389

Gene: RARB

Linked Data

• gnomAD v4: 3-25580477-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25580477C>T , CM000665.2:g.25580477C>T	GRCh38
NC_000003.11:g.25621968C>T , CM000665.1:g.25621968C>T	GRCh37
NC_000003.10:g.25596972C>T	NCBI36
NG_029013.1:g.157215C>T
NG_029013.3:g.756155C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.631-69C>T	ENSP00000373282.5:n.631-69C>T
ENST00000437042.7:c.274-69C>T	ENSP00000398840.2:n.274-69C>T
ENST00000458646.2:c.274-69C>T	ENSP00000391391.1:n.274-69C>T
ENST00000462272.6:n.555-69C>T
ENST00000479097.6:c.449-69C>T	ENSP00000508755.1:n.449-69C>T
ENST00000480001.6:c.610-69C>T	ENSP00000510647.1:n.610-69C>T
ENST00000685523.1:c.*446-69C>T	ENSP00000508765.1:n.*446-69C>T
ENST00000686715.1:c.631-69C>T	ENSP00000510539.1:n.631-69C>T
ENST00000687083.1:c.610-69C>T	ENSP00000509681.1:n.610-69C>T
ENST00000687353.1:c.631-69C>T	ENSP00000508588.1:n.631-69C>T
ENST00000687676.1:c.631-69C>T	ENSP00000510313.1:n.631-69C>T
ENST00000688892.1:c.631-69C>T	ENSP00000510650.1:n.631-69C>T
ENST00000689700.1:c.304-69C>T	ENSP00000510200.1:n.304-69C>T
ENST00000690398.1:c.*225-69C>T	ENSP00000510044.1:n.*225-69C>T
ENST00000691580.1:c.439-69C>T
ENST00000691912.1:c.610-69C>T	ENSP00000510520.1:n.610-69C>T
ENST00000693261.1:c.274-69C>T	ENSP00000508421.1:n.274-69C>T
ENST00000693580.1:c.303+10559C>T	ENSP00000510405.1:n.303+10559C>T
ENST00000330688.9:c.610-69C>T MANE Select	ENSP00000332296.4:n.610-69C>T
ENST00000330688.8:c.610-69C>T	ENSP00000332296.4:n.610-69C>T
ENST00000383772.8:c.631-69C>T	ENSP00000373282.4:n.631-69C>T
ENST00000437042.6:c.274-69C>T	ENSP00000398840.2:n.274-69C>T
ENST00000458646.1:c.274-69C>T	ENSP00000391391.1:n.274-69C>T
ENST00000462272.5:n.626-69C>T
ENST00000479097.5:n.465-69C>T
ENST00000480001.5:n.626-69C>T
NM_000965.4:c.610-69C>T	NP_000956.2:n.610-69C>T
NM_001290216.1:c.631-69C>T	NP_001277145.1:n.631-69C>T
NM_001290217.1:c.274-69C>T	NP_001277146.1:n.274-69C>T
NM_001290266.1:c.463-69C>T	NP_001277195.1:n.463-69C>T
NM_001290276.1:c.274-69C>T	NP_001277205.1:n.274-69C>T
NM_001290277.1:c.610-69C>T	NP_001277206.1:n.610-69C>T
NM_001290300.1:c.481-69C>T	NP_001277229.1:n.481-69C>T
NM_016152.3:c.274-69C>T	NP_057236.1:n.274-69C>T
NR_110892.1:n.918-69C>T
NR_110893.1:n.1079-69C>T
NM_001290216.2:c.631-69C>T	NP_001277145.1:n.631-69C>T
NM_000965.5:c.610-69C>T MANE Select	NP_000956.2:n.610-69C>T
NM_001290216.3:c.631-69C>T	NP_001277145.1:n.631-69C>T
NM_001290217.2:c.274-69C>T	NP_001277146.1:n.274-69C>T
NM_001290266.2:c.463-69C>T	NP_001277195.1:n.463-69C>T
NM_001290276.2:c.274-69C>T	NP_001277205.1:n.274-69C>T
NM_001290300.2:c.481-69C>T	NP_001277229.1:n.481-69C>T
NM_016152.4:c.274-69C>T	NP_057236.1:n.274-69C>T
NR_110892.2:n.918-69C>T
NR_110893.2:n.1079-69C>T