Canonical Allele Identifier: CA15267382

Gene: RARB

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25302124G>A , CM000665.2:g.25302124G>A	GRCh38
NC_000003.11:g.25343615G>A , CM000665.1:g.25343615G>A	GRCh37
NC_000003.10:g.25318619G>A	NCBI36
NG_029013.3:g.477802G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.178+127549G>A	ENSP00000373282.5:n.178+127549G>A
ENST00000455576.2:c.178+127549G>A	ENSP00000508527.1:n.178+127549G>A
ENST00000686715.1:c.178+127549G>A	ENSP00000510539.1:n.178+127549G>A
ENST00000687353.1:c.178+127549G>A	ENSP00000508588.1:n.178+127549G>A
ENST00000687676.1:c.178+127549G>A	ENSP00000510313.1:n.178+127549G>A
ENST00000688892.1:c.178+127549G>A	ENSP00000510650.1:n.178+127549G>A
ENST00000690398.1:c.178+127549G>A	ENSP00000510044.1:n.178+127549G>A
ENST00000383772.8:c.178+127549G>A	ENSP00000373282.4:n.178+127549G>A
NM_001290216.1:c.178+127549G>A	NP_001277145.1:n.178+127549G>A
NM_001290216.2:c.178+127549G>A	NP_001277145.1:n.178+127549G>A
NM_001290216.3:c.178+127549G>A	NP_001277145.1:n.178+127549G>A