Canonical Allele Identifier: CA467648908

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300108C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408262C>G , CM000671.2:g.134408262C>G	GRCh38
NC_000009.11:g.137300108C>G , CM000671.1:g.137300108C>G	GRCh37
NC_000009.10:g.136439929C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.393C>G MANE Select	ENSP00000419692.1:p.Thr131=
ENST00000672570.1:c.312C>G	ENSP00000500402.1:p.Thr104=
ENST00000356384.4:n.803C>G
ENST00000481739.1:c.393C>G	ENSP00000419692.1:p.Thr131=
NM_001291920.1:c.312C>G	NP_001278849.1:p.Thr104=
NM_001291921.1:c.102C>G	NP_001278850.1:p.Thr34=
NM_002957.5:c.393C>G	NP_002948.1:p.Thr131=
NM_002957.6:c.393C>G MANE Select	NP_002948.1:p.Thr131=
NM_001291921.2:c.102C>G	NP_001278850.1:p.Thr34=
NM_001291920.2:c.312C>G	NP_001278849.1:p.Thr104=