Canonical Allele Identifier: CA1352359216

Gene: RARB

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25479091C>G , CM000665.2:g.25479091C>G	GRCh38
NC_000003.11:g.25520582C>G , CM000665.1:g.25520582C>G	GRCh37
NC_000003.10:g.25495586C>G	NCBI36
NG_029013.1:g.55829C>G
NG_029013.3:g.654769C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.327+17750C>G	ENSP00000373282.5:n.327+17750C>G
ENST00000437042.7:c.-31+17750C>G	ENSP00000398840.2:n.-31+17750C>G
ENST00000455576.2:c.327+17750C>G	ENSP00000508527.1:n.327+17750C>G
ENST00000458646.2:c.-31+17750C>G	ENSP00000391391.1:n.-31+17750C>G
ENST00000462272.6:n.186+17750C>G
ENST00000479097.6:c.306+17750C>G	ENSP00000508755.1:n.306+17750C>G
ENST00000480001.6:c.306+17750C>G	ENSP00000510647.1:n.306+17750C>G
ENST00000685523.1:c.*142+17750C>G	ENSP00000508765.1:n.*142+17750C>G
ENST00000686715.1:c.327+17750C>G	ENSP00000510539.1:n.327+17750C>G
ENST00000687083.1:c.306+17750C>G	ENSP00000509681.1:n.306+17750C>G
ENST00000687353.1:c.327+17750C>G	ENSP00000508588.1:n.327+17750C>G
ENST00000687676.1:c.327+17750C>G	ENSP00000510313.1:n.327+17750C>G
ENST00000688892.1:c.327+17750C>G	ENSP00000510650.1:n.327+17750C>G
ENST00000690398.1:c.327+17750C>G	ENSP00000510044.1:n.327+17750C>G
ENST00000691580.1:c.149+17750C>G
ENST00000691912.1:c.306+17750C>G	ENSP00000510520.1:n.306+17750C>G
ENST00000693261.1:c.-31+17750C>G	ENSP00000508421.1:n.-31+17750C>G
ENST00000330688.9:c.306+17750C>G MANE Select	ENSP00000332296.4:n.306+17750C>G
ENST00000330688.8:c.306+17750C>G	ENSP00000332296.4:n.306+17750C>G
ENST00000383772.8:c.327+17750C>G	ENSP00000373282.4:n.327+17750C>G
ENST00000437042.6:c.-31+17750C>G	ENSP00000398840.2:n.-31+17750C>G
ENST00000458646.1:c.-31+17750C>G	ENSP00000391391.1:n.-31+17750C>G
ENST00000462272.5:n.322+17750C>G
ENST00000479097.5:n.322+17750C>G
ENST00000480001.5:n.322+17750C>G
NM_000965.4:c.306+17750C>G	NP_000956.2:n.306+17750C>G
NM_001290216.1:c.327+17750C>G	NP_001277145.1:n.327+17750C>G
NM_001290217.1:c.-31+17750C>G	NP_001277146.1:n.-31+17750C>G
NM_001290266.1:c.159+17750C>G	NP_001277195.1:n.159+17750C>G
NM_001290276.1:c.-31+17750C>G	NP_001277205.1:n.-31+17750C>G
NM_001290277.1:c.306+17750C>G	NP_001277206.1:n.306+17750C>G
NM_001290300.1:c.177+17750C>G	NP_001277229.1:n.177+17750C>G
NM_016152.3:c.-31+17750C>G	NP_057236.1:n.-31+17750C>G
NR_110892.1:n.775+17750C>G
NR_110893.1:n.775+17750C>G
NM_001290216.2:c.327+17750C>G	NP_001277145.1:n.327+17750C>G
NM_000965.5:c.306+17750C>G MANE Select	NP_000956.2:n.306+17750C>G
NM_001290216.3:c.327+17750C>G	NP_001277145.1:n.327+17750C>G
NM_001290217.2:c.-31+17750C>G	NP_001277146.1:n.-31+17750C>G
NM_001290266.2:c.159+17750C>G	NP_001277195.1:n.159+17750C>G
NM_001290276.2:c.-31+17750C>G	NP_001277205.1:n.-31+17750C>G
NM_001290300.2:c.177+17750C>G	NP_001277229.1:n.177+17750C>G
NM_016152.4:c.-31+17750C>G	NP_057236.1:n.-31+17750C>G
NR_110892.2:n.775+17750C>G
NR_110893.2:n.775+17750C>G