Canonical Allele Identifier: CA467649090

Gene: RXRA

Linked Data

• dbSNP Id: rs1481124879
• gnomAD v2: 9-137300144-A-G
• gnomAD v4: 9-134408298-A-G
• MyVariant Identifiers: chr9:g.137300144A>G (hg19) ; chr9:g.134408298A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408298A>G , CM000671.2:g.134408298A>G	GRCh38
NC_000009.11:g.137300144A>G , CM000671.1:g.137300144A>G	GRCh37
NC_000009.10:g.136439965A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.429A>G MANE Select	ENSP00000419692.1:p.Ser143=
ENST00000672570.1:c.348A>G	ENSP00000500402.1:p.Ser116=
ENST00000356384.4:n.839A>G
ENST00000481739.1:c.429A>G	ENSP00000419692.1:p.Ser143=
NM_001291920.1:c.348A>G	NP_001278849.1:p.Ser116=
NM_001291921.1:c.138A>G	NP_001278850.1:p.Ser46=
NM_002957.5:c.429A>G	NP_002948.1:p.Ser143=
NM_002957.6:c.429A>G MANE Select	NP_002948.1:p.Ser143=
NM_001291921.2:c.138A>G	NP_001278850.1:p.Ser46=
NM_001291920.2:c.348A>G	NP_001278849.1:p.Ser116=