Canonical Allele Identifier: CA1129841849

Gene: RXRA

Linked Data

• dbSNP Id: rs887819380
• gnomAD v3: 9-134409889-T-G
• gnomAD v4: 9-134409889-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134409889T>G , CM000671.2:g.134409889T>G	GRCh38
NC_000009.11:g.137301735T>G , CM000671.1:g.137301735T>G	GRCh37
NC_000009.10:g.136441556T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.610+770T>G MANE Select	ENSP00000419692.1:n.610+770T>G
ENST00000672570.1:c.529+770T>G	ENSP00000500402.1:n.529+770T>G
ENST00000356384.4:n.1020+770T>G
ENST00000481739.1:c.610+770T>G	ENSP00000419692.1:n.610+770T>G
NM_001291920.1:c.529+770T>G	NP_001278849.1:n.529+770T>G
NM_001291921.1:c.319+770T>G	NP_001278850.1:n.319+770T>G
NM_002957.5:c.610+770T>G	NP_002948.1:n.610+770T>G
NM_002957.6:c.610+770T>G MANE Select	NP_002948.1:n.610+770T>G
NM_001291921.2:c.319+770T>G	NP_001278850.1:n.319+770T>G
NM_001291920.2:c.529+770T>G	NP_001278849.1:n.529+770T>G