Canonical Allele Identifier: CA5317725

Gene: RXRA

Linked Data

• dbSNP Id: rs770018441
• ExAC: 9:137300124 A / G
• gnomAD v2: 9-137300124-A-G
• gnomAD v4: 9-134408278-A-G
• MyVariant Identifiers: chr9:g.137300124A>G (hg19) ; chr9:g.134408278A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408278A>G , CM000671.2:g.134408278A>G	GRCh38
NC_000009.11:g.137300124A>G , CM000671.1:g.137300124A>G	GRCh37
NC_000009.10:g.136439945A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.409A>G MANE Select	ENSP00000419692.1:p.Ile137Val
ENST00000672570.1:c.328A>G	ENSP00000500402.1:p.Ile110Val
ENST00000356384.4:n.819A>G
ENST00000481739.1:c.409A>G	ENSP00000419692.1:p.Ile137Val
NM_001291920.1:c.328A>G	NP_001278849.1:p.Ile110Val
NM_001291921.1:c.118A>G	NP_001278850.1:p.Ile40Val
NM_002957.5:c.409A>G	NP_002948.1:p.Ile137Val
NM_002957.6:c.409A>G MANE Select	NP_002948.1:p.Ile137Val
NM_001291921.2:c.118A>G	NP_001278850.1:p.Ile40Val
NM_001291920.2:c.328A>G	NP_001278849.1:p.Ile110Val