Canonical Allele Identifier: CA201041295

Gene: RXRA

Linked Data

• dbSNP Id: rs564830401
• gnomAD v3: 9-134409950-A-G
• gnomAD v4: 9-134409950-A-G
• MyVariant Identifiers: chr9:g.137301796A>G (hg19) ; chr9:g.134409950A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409950A>G , CM000671.2:g.134409950A>G	GRCh38
NC_000009.11:g.137301796A>G , CM000671.1:g.137301796A>G	GRCh37
NC_000009.10:g.136441617A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.610+831A>G MANE Select	ENSP00000419692.1:n.610+831A>G
ENST00000672570.1:c.529+831A>G	ENSP00000500402.1:n.529+831A>G
ENST00000356384.4:n.1020+831A>G
ENST00000481739.1:c.610+831A>G	ENSP00000419692.1:n.610+831A>G
NM_001291920.1:c.529+831A>G	NP_001278849.1:n.529+831A>G
NM_001291921.1:c.319+831A>G	NP_001278850.1:n.319+831A>G
NM_002957.5:c.610+831A>G	NP_002948.1:n.610+831A>G
NM_002957.6:c.610+831A>G MANE Select	NP_002948.1:n.610+831A>G
NM_001291921.2:c.319+831A>G	NP_001278850.1:n.319+831A>G
NM_001291920.2:c.529+831A>G	NP_001278849.1:n.529+831A>G