Canonical Allele Identifier: CA351896823

Gene: RARB

Linked Data

• dbSNP Id: rs373578752
• gnomAD v3: 3-25580582-G-T
• gnomAD v4: 3-25580582-G-T
• MyVariant Identifiers: chr3:g.25622073G>T (hg19) ; chr3:g.25580582G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25580582G>T , CM000665.2:g.25580582G>T	GRCh38
NC_000003.11:g.25622073G>T , CM000665.1:g.25622073G>T	GRCh37
NC_000003.10:g.25597077G>T	NCBI36
NG_029013.1:g.157320G>T
NG_029013.3:g.756260G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000383772.9:c.667G>T	ENSP00000373282.5:p.Gly223Cys
ENST00000437042.7:c.310G>T	ENSP00000398840.2:p.Gly104Cys
ENST00000458646.2:c.310G>T	ENSP00000391391.1:p.Gly104Cys
ENST00000462272.6:n.591G>T
ENST00000479097.6:c.*35G>T	ENSP00000508755.1:n.*35G>T
ENST00000480001.6:c.646G>T	ENSP00000510647.1:p.Gly216Cys
ENST00000685523.1:c.*482G>T	ENSP00000508765.1:n.*482G>T
ENST00000686715.1:c.667G>T	ENSP00000510539.1:p.Gly223Cys
ENST00000687083.1:c.646G>T	ENSP00000509681.1:p.Gly216Cys
ENST00000687353.1:c.667G>T	ENSP00000508588.1:p.Gly223Cys
ENST00000687676.1:c.667G>T	ENSP00000510313.1:p.Gly223Cys
ENST00000688892.1:c.667G>T	ENSP00000510650.1:p.Gly223Cys
ENST00000689700.1:c.340G>T	ENSP00000510200.1:p.Gly114Cys
ENST00000690398.1:c.*261G>T	ENSP00000510044.1:n.*261G>T
ENST00000691580.1:c.475G>T
ENST00000691912.1:c.646G>T	ENSP00000510520.1:p.Gly216Cys
ENST00000693261.1:c.310G>T	ENSP00000508421.1:p.Gly104Cys
ENST00000693580.1:c.303+10664G>T	ENSP00000510405.1:n.303+10664G>T
ENST00000330688.9:c.646G>T MANE Select	ENSP00000332296.4:p.Gly216Cys
ENST00000330688.8:c.646G>T	ENSP00000332296.4:p.Gly216Cys
ENST00000383772.8:c.667G>T	ENSP00000373282.4:p.Gly223Cys
ENST00000437042.6:c.310G>T	ENSP00000398840.2:p.Gly104Cys
ENST00000458646.1:c.310G>T	ENSP00000391391.1:p.Gly104Cys
ENST00000462272.5:n.662G>T
ENST00000479097.5:n.501G>T
ENST00000480001.5:n.662G>T
NM_000965.4:c.646G>T	NP_000956.2:p.Gly216Cys
NM_001290216.1:c.667G>T	NP_001277145.1:p.Gly223Cys
NM_001290217.1:c.310G>T	NP_001277146.1:p.Gly104Cys
NM_001290266.1:c.499G>T	NP_001277195.1:p.Gly167Cys
NM_001290276.1:c.310G>T	NP_001277205.1:p.Gly104Cys
NM_001290277.1:c.646G>T	NP_001277206.1:p.Gly216Cys
NM_001290300.1:c.517G>T	NP_001277229.1:p.Gly173Cys
NM_016152.3:c.310G>T	NP_057236.1:p.Gly104Cys
NR_110892.1:n.954G>T
NR_110893.1:n.1115G>T
NM_001290216.2:c.667G>T	NP_001277145.1:p.Gly223Cys
NM_000965.5:c.646G>T MANE Select	NP_000956.2:p.Gly216Cys
NM_001290216.3:c.667G>T	NP_001277145.1:p.Gly223Cys
NM_001290217.2:c.310G>T	NP_001277146.1:p.Gly104Cys
NM_001290266.2:c.499G>T	NP_001277195.1:p.Gly167Cys
NM_001290276.2:c.310G>T	NP_001277205.1:p.Gly104Cys
NM_001290300.2:c.517G>T	NP_001277229.1:p.Gly173Cys
NM_016152.4:c.310G>T	NP_057236.1:p.Gly104Cys
NR_110892.2:n.954G>T
NR_110893.2:n.1115G>T