Canonical Allele Identifier: CA13021831

Gene: RXRA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134368146T>C , CM000671.2:g.134368146T>C	GRCh38
NC_000009.11:g.137259992T>C , CM000671.1:g.137259992T>C	GRCh37
NC_000009.10:g.136399813T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.29-33486T>C MANE Select	ENSP00000419692.1:n.29-33486T>C
ENST00000481739.1:c.29-33486T>C	ENSP00000419692.1:n.29-33486T>C
ENST00000484822.1:n.453-33486T>C
NM_002957.5:c.29-33486T>C	NP_002948.1:n.29-33486T>C
NM_002957.6:c.29-33486T>C MANE Select	NP_002948.1:n.29-33486T>C