Canonical Allele Identifier: CA1883176839

Gene: RXRA

Linked Data

• dbSNP Id: rs1588293592

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408329T>G , CM000671.2:g.134408329T>G	GRCh38
NC_000009.11:g.137300175T>G , CM000671.1:g.137300175T>G	GRCh37
NC_000009.10:g.136439996T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+30T>G MANE Select	ENSP00000419692.1:n.430+30T>G
ENST00000672570.1:c.349+30T>G	ENSP00000500402.1:n.349+30T>G
ENST00000356384.4:n.840+30T>G
ENST00000481739.1:c.430+30T>G	ENSP00000419692.1:n.430+30T>G
NM_001291920.1:c.349+30T>G	NP_001278849.1:n.349+30T>G
NM_001291921.1:c.139+30T>G	NP_001278850.1:n.139+30T>G
NM_002957.5:c.430+30T>G	NP_002948.1:n.430+30T>G
NM_002957.6:c.430+30T>G MANE Select	NP_002948.1:n.430+30T>G
NM_001291921.2:c.139+30T>G	NP_001278850.1:n.139+30T>G
NM_001291920.2:c.349+30T>G	NP_001278849.1:n.349+30T>G