Canonical Allele Identifier: CA375451975

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408159-C-G
• MyVariant Identifiers: chr9:g.137300005C>G (hg19) ; chr9:g.134408159C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408159C>G , CM000671.2:g.134408159C>G	GRCh38
NC_000009.11:g.137300005C>G , CM000671.1:g.137300005C>G	GRCh37
NC_000009.10:g.136439826C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.290C>G MANE Select	ENSP00000419692.1:p.Pro97Arg
ENST00000672570.1:c.209C>G	ENSP00000500402.1:p.Pro70Arg
ENST00000356384.4:n.700C>G
ENST00000481739.1:c.290C>G	ENSP00000419692.1:p.Pro97Arg
NM_001291920.1:c.209C>G	NP_001278849.1:p.Pro70Arg
NM_001291921.1:c.-2C>G	NP_001278850.1:n.-2C>G
NM_002957.5:c.290C>G	NP_002948.1:p.Pro97Arg
NM_002957.6:c.290C>G MANE Select	NP_002948.1:p.Pro97Arg
NM_001291921.2:c.-2C>G	NP_001278850.1:n.-2C>G
NM_001291920.2:c.209C>G	NP_001278849.1:p.Pro70Arg