Canonical Allele Identifier: CA860857901
Gene: RXRA HGNC NCBI

Linked Data

dbSNP Id: rs1216845379

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.134410070G>A , CM000671.2:g.134410070G>A GRCh38
NC_000009.11:g.137301916G>A , CM000671.1:g.137301916G>A GRCh37
NC_000009.10:g.136441737G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000481739.2:c.610+951G>A MANE Select ENSP00000419692.1:n.610+951G>A
ENST00000672570.1:c.529+951G>A ENSP00000500402.1:n.529+951G>A
ENST00000356384.4:n.1020+951G>A
ENST00000481739.1:c.610+951G>A ENSP00000419692.1:n.610+951G>A
NM_001291920.1:c.529+951G>A NP_001278849.1:n.529+951G>A
NM_001291921.1:c.319+951G>A NP_001278850.1:n.319+951G>A
NM_002957.5:c.610+951G>A NP_002948.1:n.610+951G>A
NM_002957.6:c.610+951G>A MANE Select NP_002948.1:n.610+951G>A
NM_001291921.2:c.319+951G>A NP_001278850.1:n.319+951G>A
NM_001291920.2:c.529+951G>A NP_001278849.1:n.529+951G>A