Canonical Allele Identifier: CA15241831

Gene: RARB

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25129806T>C , CM000665.2:g.25129806T>C	GRCh38
NC_000003.11:g.25171297T>C , CM000665.1:g.25171297T>C	GRCh37
NC_000003.10:g.25146301T>C	NCBI36
NG_029013.3:g.305484T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.-327-2355T>C	ENSP00000373282.5:n.-327-2355T>C
ENST00000455576.2:c.-279-44313T>C	ENSP00000508527.1:n.-279-44313T>C
ENST00000686715.1:c.-279-44313T>C	ENSP00000510539.1:n.-279-44313T>C
ENST00000687353.1:c.-279-44313T>C	ENSP00000508588.1:n.-279-44313T>C
ENST00000687676.1:c.-279-44313T>C	ENSP00000510313.1:n.-279-44313T>C
ENST00000688892.1:c.-279-44313T>C	ENSP00000510650.1:n.-279-44313T>C
NM_001290216.2:c.-279-44313T>C	NP_001277145.1:n.-279-44313T>C
NM_001290216.3:c.-279-44313T>C	NP_001277145.1:n.-279-44313T>C