Canonical Allele Identifier: CA351896843
Gene: RARB HGNC NCBI

Linked Data

dbSNP Id: rs1701132764

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.25580585C>T , CM000665.2:g.25580585C>T GRCh38
NC_000003.11:g.25622076C>T , CM000665.1:g.25622076C>T GRCh37
NC_000003.10:g.25597080C>T NCBI36
NG_029013.1:g.157323C>T
NG_029013.3:g.756263C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000383772.9:c.670C>T ENSP00000373282.5:p.Leu224Phe
ENST00000437042.7:c.313C>T ENSP00000398840.2:p.Leu105Phe
ENST00000458646.2:c.313C>T ENSP00000391391.1:p.Leu105Phe
ENST00000462272.6:n.594C>T
ENST00000479097.6:c.*38C>T ENSP00000508755.1:n.*38C>T
ENST00000480001.6:c.649C>T ENSP00000510647.1:p.Leu217Phe
ENST00000685523.1:c.*485C>T ENSP00000508765.1:n.*485C>T
ENST00000686715.1:c.670C>T ENSP00000510539.1:p.Leu224Phe
ENST00000687083.1:c.649C>T ENSP00000509681.1:p.Leu217Phe
ENST00000687353.1:c.670C>T ENSP00000508588.1:p.Leu224Phe
ENST00000687676.1:c.670C>T ENSP00000510313.1:p.Leu224Phe
ENST00000688892.1:c.670C>T ENSP00000510650.1:p.Leu224Phe
ENST00000689700.1:c.343C>T ENSP00000510200.1:p.Leu115Phe
ENST00000690398.1:c.*264C>T ENSP00000510044.1:n.*264C>T
ENST00000691580.1:c.478C>T
ENST00000691912.1:c.649C>T ENSP00000510520.1:p.Leu217Phe
ENST00000693261.1:c.313C>T ENSP00000508421.1:p.Leu105Phe
ENST00000693580.1:c.303+10667C>T ENSP00000510405.1:n.303+10667C>T
ENST00000330688.9:c.649C>T MANE Select ENSP00000332296.4:p.Leu217Phe
ENST00000330688.8:c.649C>T ENSP00000332296.4:p.Leu217Phe
ENST00000383772.8:c.670C>T ENSP00000373282.4:p.Leu224Phe
ENST00000437042.6:c.313C>T ENSP00000398840.2:p.Leu105Phe
ENST00000458646.1:c.313C>T ENSP00000391391.1:p.Leu105Phe
ENST00000462272.5:n.665C>T
ENST00000479097.5:n.504C>T
ENST00000480001.5:n.665C>T
NM_000965.4:c.649C>T NP_000956.2:p.Leu217Phe
NM_001290216.1:c.670C>T NP_001277145.1:p.Leu224Phe
NM_001290217.1:c.313C>T NP_001277146.1:p.Leu105Phe
NM_001290266.1:c.502C>T NP_001277195.1:p.Leu168Phe
NM_001290276.1:c.313C>T NP_001277205.1:p.Leu105Phe
NM_001290277.1:c.649C>T NP_001277206.1:p.Leu217Phe
NM_001290300.1:c.520C>T NP_001277229.1:p.Leu174Phe
NM_016152.3:c.313C>T NP_057236.1:p.Leu105Phe
NR_110892.1:n.957C>T
NR_110893.1:n.1118C>T
NM_001290216.2:c.670C>T NP_001277145.1:p.Leu224Phe
NM_000965.5:c.649C>T MANE Select NP_000956.2:p.Leu217Phe
NM_001290216.3:c.670C>T NP_001277145.1:p.Leu224Phe
NM_001290217.2:c.313C>T NP_001277146.1:p.Leu105Phe
NM_001290266.2:c.502C>T NP_001277195.1:p.Leu168Phe
NM_001290276.2:c.313C>T NP_001277205.1:p.Leu105Phe
NM_001290300.2:c.520C>T NP_001277229.1:p.Leu174Phe
NM_016152.4:c.313C>T NP_057236.1:p.Leu105Phe
NR_110892.2:n.957C>T
NR_110893.2:n.1118C>T