Canonical Allele Identifier: CA860853297

Gene: RXRA

Linked Data

• dbSNP Id: rs12004589
• gnomAD v3: 9-134398879-G-A
• gnomAD v4: 9-134398879-G-A
• MyVariant Identifiers: chr9:g.137290725G>A (hg19) ; chr9:g.134398879G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134398879G>A , CM000671.2:g.134398879G>A	GRCh38
NC_000009.11:g.137290725G>A , CM000671.1:g.137290725G>A	GRCh37
NC_000009.10:g.136430546G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.29-2753G>A MANE Select	ENSP00000419692.1:n.29-2753G>A
ENST00000649020.1:c.119-2753G>A	ENSP00000497073.1:n.119-2753G>A
ENST00000672570.1:c.-53-2753G>A	ENSP00000500402.1:n.-53-2753G>A
ENST00000356384.4:n.294-2517G>A
ENST00000481739.1:c.29-2753G>A	ENSP00000419692.1:n.29-2753G>A
ENST00000484822.1:n.453-2753G>A
NM_001291920.1:c.-53-2753G>A	NP_001278849.1:n.-53-2753G>A
NM_002957.5:c.29-2753G>A	NP_002948.1:n.29-2753G>A
NM_002957.6:c.29-2753G>A MANE Select	NP_002948.1:n.29-2753G>A
NM_001291920.2:c.-53-2753G>A	NP_001278849.1:n.-53-2753G>A