Canonical Allele Identifier: CA375452628

Gene: RXRA

Linked Data

• dbSNP Id: rs1163418709
• gnomAD v3: 9-134408269-A-G
• gnomAD v4: 9-134408269-A-G
• MyVariant Identifiers: chr9:g.137300115A>G (hg19) ; chr9:g.134408269A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408269A>G , CM000671.2:g.134408269A>G	GRCh38
NC_000009.11:g.137300115A>G , CM000671.1:g.137300115A>G	GRCh37
NC_000009.10:g.136439936A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.400A>G MANE Select	ENSP00000419692.1:p.Ile134Val
ENST00000672570.1:c.319A>G	ENSP00000500402.1:p.Ile107Val
ENST00000356384.4:n.810A>G
ENST00000481739.1:c.400A>G	ENSP00000419692.1:p.Ile134Val
NM_001291920.1:c.319A>G	NP_001278849.1:p.Ile107Val
NM_001291921.1:c.109A>G	NP_001278850.1:p.Ile37Val
NM_002957.5:c.400A>G	NP_002948.1:p.Ile134Val
NM_002957.6:c.400A>G MANE Select	NP_002948.1:p.Ile134Val
NM_001291921.2:c.109A>G	NP_001278850.1:p.Ile37Val
NM_001291920.2:c.319A>G	NP_001278849.1:p.Ile107Val