Canonical Allele Identifier: CA467648771

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408238-C-A
• MyVariant Identifiers: chr9:g.137300084C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408238C>A , CM000671.2:g.134408238C>A	GRCh38
NC_000009.11:g.137300084C>A , CM000671.1:g.137300084C>A	GRCh37
NC_000009.10:g.136439905C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.369C>A MANE Select	ENSP00000419692.1:p.Pro123=
ENST00000672570.1:c.288C>A	ENSP00000500402.1:p.Pro96=
ENST00000356384.4:n.779C>A
ENST00000481739.1:c.369C>A	ENSP00000419692.1:p.Pro123=
NM_001291920.1:c.288C>A	NP_001278849.1:p.Pro96=
NM_001291921.1:c.78C>A	NP_001278850.1:p.Pro26=
NM_002957.5:c.369C>A	NP_002948.1:p.Pro123=
NM_002957.6:c.369C>A MANE Select	NP_002948.1:p.Pro123=
NM_001291921.2:c.78C>A	NP_001278850.1:p.Pro26=
NM_001291920.2:c.288C>A	NP_001278849.1:p.Pro96=