Canonical Allele Identifier: CA432834474
Gene: RARB HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.25622078C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.25580587C>A , CM000665.2:g.25580587C>A GRCh38
NC_000003.11:g.25622078C>A , CM000665.1:g.25622078C>A GRCh37
NC_000003.10:g.25597082C>A NCBI36
NG_029013.1:g.157325C>A
NG_029013.3:g.756265C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000383772.9:c.672C>A ENSP00000373282.5:p.Leu224=
ENST00000437042.7:c.315C>A ENSP00000398840.2:p.Leu105=
ENST00000458646.2:c.315C>A ENSP00000391391.1:p.Leu105=
ENST00000462272.6:n.596C>A
ENST00000479097.6:c.*40C>A ENSP00000508755.1:n.*40C>A
ENST00000480001.6:c.651C>A ENSP00000510647.1:p.Leu217=
ENST00000685523.1:c.*487C>A ENSP00000508765.1:n.*487C>A
ENST00000686715.1:c.672C>A ENSP00000510539.1:p.Leu224=
ENST00000687083.1:c.651C>A ENSP00000509681.1:p.Leu217=
ENST00000687353.1:c.672C>A ENSP00000508588.1:p.Leu224=
ENST00000687676.1:c.672C>A ENSP00000510313.1:p.Leu224=
ENST00000688892.1:c.672C>A ENSP00000510650.1:p.Leu224=
ENST00000689700.1:c.345C>A ENSP00000510200.1:p.Leu115=
ENST00000690398.1:c.*266C>A ENSP00000510044.1:n.*266C>A
ENST00000691580.1:c.480C>A
ENST00000691912.1:c.651C>A ENSP00000510520.1:p.Leu217=
ENST00000693261.1:c.315C>A ENSP00000508421.1:p.Leu105=
ENST00000693580.1:c.303+10669C>A ENSP00000510405.1:n.303+10669C>A
ENST00000330688.9:c.651C>A MANE Select ENSP00000332296.4:p.Leu217=
ENST00000330688.8:c.651C>A ENSP00000332296.4:p.Leu217=
ENST00000383772.8:c.672C>A ENSP00000373282.4:p.Leu224=
ENST00000437042.6:c.315C>A ENSP00000398840.2:p.Leu105=
ENST00000458646.1:c.315C>A ENSP00000391391.1:p.Leu105=
ENST00000462272.5:n.667C>A
ENST00000479097.5:n.506C>A
ENST00000480001.5:n.667C>A
NM_000965.4:c.651C>A NP_000956.2:p.Leu217=
NM_001290216.1:c.672C>A NP_001277145.1:p.Leu224=
NM_001290217.1:c.315C>A NP_001277146.1:p.Leu105=
NM_001290266.1:c.504C>A NP_001277195.1:p.Leu168=
NM_001290276.1:c.315C>A NP_001277205.1:p.Leu105=
NM_001290277.1:c.651C>A NP_001277206.1:p.Leu217=
NM_001290300.1:c.522C>A NP_001277229.1:p.Leu174=
NM_016152.3:c.315C>A NP_057236.1:p.Leu105=
NR_110892.1:n.959C>A
NR_110893.1:n.1120C>A
NM_001290216.2:c.672C>A NP_001277145.1:p.Leu224=
NM_000965.5:c.651C>A MANE Select NP_000956.2:p.Leu217=
NM_001290216.3:c.672C>A NP_001277145.1:p.Leu224=
NM_001290217.2:c.315C>A NP_001277146.1:p.Leu105=
NM_001290266.2:c.504C>A NP_001277195.1:p.Leu168=
NM_001290276.2:c.315C>A NP_001277205.1:p.Leu105=
NM_001290300.2:c.522C>A NP_001277229.1:p.Leu174=
NM_016152.4:c.315C>A NP_057236.1:p.Leu105=
NR_110892.2:n.959C>A
NR_110893.2:n.1120C>A