Canonical Allele Identifier: CA201073160
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs973984873

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134398814A>G , CM000671.2:g.134398814A>G GRCh38
NC_000009.11:g.137290660A>G , CM000671.1:g.137290660A>G GRCh37
NC_000009.10:g.136430481A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000481739.2:c.29-2818A>G MANE Select ENSP00000419692.1:n.29-2818A>G
ENST00000649020.1:c.119-2818A>G ENSP00000497073.1:n.119-2818A>G
ENST00000672570.1:c.-53-2818A>G ENSP00000500402.1:n.-53-2818A>G
ENST00000356384.4:n.294-2582A>G
ENST00000481739.1:c.29-2818A>G ENSP00000419692.1:n.29-2818A>G
ENST00000484822.1:n.453-2818A>G
NM_001291920.1:c.-53-2818A>G NP_001278849.1:n.-53-2818A>G
NM_002957.5:c.29-2818A>G NP_002948.1:n.29-2818A>G
NM_002957.6:c.29-2818A>G MANE Select NP_002948.1:n.29-2818A>G
NM_001291920.2:c.-53-2818A>G NP_001278849.1:n.-53-2818A>G