Canonical Allele Identifier: CA5317729

Gene: RXRA

Linked Data

• dbSNP Id: rs540273274
• ExAC: 9:137300137 G / A
• gnomAD v2: 9-137300137-G-A
• gnomAD v3: 9-134408291-G-A
• gnomAD v4: 9-134408291-G-A
• MyVariant Identifiers: chr9:g.137300137G>A (hg19) ; chr9:g.134408291G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408291G>A , CM000671.2:g.134408291G>A	GRCh38
NC_000009.11:g.137300137G>A , CM000671.1:g.137300137G>A	GRCh37
NC_000009.10:g.136439958G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.422G>A MANE Select	ENSP00000419692.1:p.Arg141His
ENST00000672570.1:c.341G>A	ENSP00000500402.1:p.Arg114His
ENST00000356384.4:n.832G>A
ENST00000481739.1:c.422G>A	ENSP00000419692.1:p.Arg141His
NM_001291920.1:c.341G>A	NP_001278849.1:p.Arg114His
NM_001291921.1:c.131G>A	NP_001278850.1:p.Arg44His
NM_002957.5:c.422G>A	NP_002948.1:p.Arg141His
NM_002957.6:c.422G>A MANE Select	NP_002948.1:p.Arg141His
NM_001291921.2:c.131G>A	NP_001278850.1:p.Arg44His
NM_001291920.2:c.341G>A	NP_001278849.1:p.Arg114His