Canonical Allele Identifier: CA1883176625

Gene: RXRA

Linked Data

• dbSNP Id: rs1831081945

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134407933C>G , CM000671.2:g.134407933C>G	GRCh38
NC_000009.11:g.137299779C>G , CM000671.1:g.137299779C>G	GRCh37
NC_000009.10:g.136439600C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.280-216C>G MANE Select	ENSP00000419692.1:n.280-216C>G
ENST00000672570.1:c.199-216C>G	ENSP00000500402.1:n.199-216C>G
ENST00000356384.4:n.690-216C>G
ENST00000481739.1:c.280-216C>G	ENSP00000419692.1:n.280-216C>G
NM_001291920.1:c.199-216C>G	NP_001278849.1:n.199-216C>G
NM_001291921.1:c.-12-216C>G	NP_001278850.1:n.-12-216C>G
NM_002957.5:c.280-216C>G	NP_002948.1:n.280-216C>G
NM_002957.6:c.280-216C>G MANE Select	NP_002948.1:n.280-216C>G
NM_001291921.2:c.-12-216C>G	NP_001278850.1:n.-12-216C>G
NM_001291920.2:c.199-216C>G	NP_001278849.1:n.199-216C>G