Canonical Allele Identifier: CA1883177702
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1588294902

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134409966T>G , CM000671.2:g.134409966T>G GRCh38
NC_000009.11:g.137301812T>G , CM000671.1:g.137301812T>G GRCh37
NC_000009.10:g.136441633T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.610+847T>G MANE Select ENSP00000419692.1:n.610+847T>G
ENST00000672570.1:c.529+847T>G ENSP00000500402.1:n.529+847T>G
ENST00000356384.4:n.1020+847T>G
ENST00000481739.1:c.610+847T>G ENSP00000419692.1:n.610+847T>G
NM_001291920.1:c.529+847T>G NP_001278849.1:n.529+847T>G
NM_001291921.1:c.319+847T>G NP_001278850.1:n.319+847T>G
NM_002957.5:c.610+847T>G NP_002948.1:n.610+847T>G
NM_002957.6:c.610+847T>G MANE Select NP_002948.1:n.610+847T>G
NM_001291921.2:c.319+847T>G NP_001278850.1:n.319+847T>G
NM_001291920.2:c.529+847T>G NP_001278849.1:n.529+847T>G