Canonical Allele Identifier: CA1129836426

Gene: RXRA

Linked Data

• dbSNP Id: rs1831542193
• gnomAD v3: 9-134432123-C-G
• gnomAD v4: 9-134432123-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134432123C>G , CM000671.2:g.134432123C>G	GRCh38
NC_000009.11:g.137323969C>G , CM000671.1:g.137323969C>G	GRCh37
NC_000009.10:g.136463790C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000481739.2:c.1135+127C>G MANE Select	ENSP00000419692.1:n.1135+127C>G
ENST00000672570.1:c.1054+127C>G	ENSP00000500402.1:n.1054+127C>G
ENST00000356384.4:n.1545+127C>G
ENST00000481739.1:c.1135+127C>G	ENSP00000419692.1:n.1135+127C>G
NM_001291920.1:c.1054+127C>G	NP_001278849.1:n.1054+127C>G
NM_001291921.1:c.844+127C>G	NP_001278850.1:n.844+127C>G
NM_002957.5:c.1135+127C>G	NP_002948.1:n.1135+127C>G
NM_002957.6:c.1135+127C>G MANE Select	NP_002948.1:n.1135+127C>G
NM_001291921.2:c.844+127C>G	NP_001278850.1:n.844+127C>G
NM_001291920.2:c.1054+127C>G	NP_001278849.1:n.1054+127C>G