Canonical Allele Identifier: CA1352131578

Gene: RARB

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25070680C>G , CM000665.2:g.25070680C>G	GRCh38
NC_000003.11:g.25112171C>G , CM000665.1:g.25112171C>G	GRCh37
NC_000003.10:g.25087175C>G	NCBI36
NG_029013.3:g.246358C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.-328+10504C>G	ENSP00000373282.5:n.-328+10504C>G
ENST00000455576.2:c.-280+10504C>G	ENSP00000508527.1:n.-280+10504C>G
ENST00000686715.1:c.-400-5483C>G	ENSP00000510539.1:n.-400-5483C>G
ENST00000687353.1:c.-400-5483C>G	ENSP00000508588.1:n.-400-5483C>G
ENST00000687512.1:n.131+10504C>G
ENST00000687676.1:c.-280+10504C>G	ENSP00000510313.1:n.-280+10504C>G
ENST00000688892.1:c.-280+10504C>G	ENSP00000510650.1:n.-280+10504C>G
XR_245195.2:n.191+10504C>G
NM_001290216.2:c.-280+10504C>G	NP_001277145.1:n.-280+10504C>G
NM_001290216.3:c.-280+10504C>G	NP_001277145.1:n.-280+10504C>G